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Chromosome banding in amphibia
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/aja.1000760103openalex-snapshot
Sex determination in ambystomid salamanders: A study of the progeny of females experimentally converted into males
inferredcites →https://doi.org/10.1002/jez.1400790104openalex-snapshot
Sex differentiation in a haploid salamander, Triton taeniatus Laur
inferredcites →https://doi.org/10.1002/jez.1401340105openalex-snapshot
Male homogamety in the Mexican axolotl: A study of the progeny obtained when germ cells of a genetic male are incorporated in a developing ovary
inferredcites →https://doi.org/10.1002/jez.1401420118openalex-snapshot
The origin of spontaneous heteroploids in the progeny of diploid, triploid, and tetraploid axolotl females
inferredcites →https://doi.org/10.1002/jmor.1050980106openalex-snapshot
Structure and functional capacity of the ovaries of higher polyploids (4N, 5N) in the Mexican axolotl (Siredon or Ambystoma mexicanum)
inferredcites →https://doi.org/10.1007/978-1-4613-4470-4_5openalex-snapshot
Working Maps of the Lampbrush Chromosomes of Amphibia
inferredcites →https://doi.org/10.1007/978-1-4757-6781-0_14openalex-snapshot
Cytotaxonomy and Cytogenetics in European Newt Species
inferredcites →https://doi.org/10.1007/978-1-4757-6781-0_4openalex-snapshot
Aspects of the Reproductive Biology of Japanese Anurans
inferredcites →https://doi.org/10.1007/978-3-642-88178-7openalex-snapshot
Sex Chromosomes and Sex-Linked Genes
inferredcites →https://doi.org/10.1007/bf00125283openalex-snapshot
Cytotaxonomy of the Ranidae, Rhacophoridae, Hyperoliidae (Anura) from Madagascar with a note on the karyotype of two amphibians of the Seychelles
inferredcites →https://doi.org/10.1007/bf00284881openalex-snapshot
Fluorometric properties of the bibenzimidazole derivative hoechst 33258, a fluorescent probe specific for AT concentration in chromosomal DNA
inferredcites →https://doi.org/10.1007/bf00284942openalex-snapshot
Evolution of sex-chromosomes and formation of W-chromatin in snakes
inferredcites →https://doi.org/10.1007/bf00290995openalex-snapshot
Cytological differentiation of constitutive heterochromatin
inferredcites →https://doi.org/10.1007/bf00291027openalex-snapshot
Chromosome complements of the genus Xenopus
inferredcites →https://doi.org/10.1007/bf00293907openalex-snapshot
DNS-Gehalt und Chromosomenstruktur bei Amphibien
inferredcites →https://doi.org/10.1007/bf00319994openalex-snapshot
Close karyological kinship between the reptilian suborder serpentes and the class aves
inferredcites →https://doi.org/10.1007/bf00321223openalex-snapshot
The maps of the lampbrush chromosomes of Triturus (Amphibia urodela)
inferredcites →https://doi.org/10.1007/bf00327708openalex-snapshot
Satellite DNA and evolution of sex chromosomes
inferredcites →https://doi.org/10.1007/bf00330555openalex-snapshot
Absence of chiasmata from the heteromorphic region of chromosome I during spermatogenesis in Triturus cristatus carnifex
inferredcites →https://doi.org/10.1007/bf00331833openalex-snapshot
Localisation et signification des zones Q observ�es sur les chromosomes mitotiques de l'amphibien Pleurodeles waltlii Michah. apr�s coloration par la moutarde de quinacrine
inferredcites →https://doi.org/10.1007/bf00399425openalex-snapshot
Banding patterns in newt chromosomes by the giemsa stain
inferredcites →https://doi.org/10.1007/bf01931894openalex-snapshot
Structural correspondence between nucleolus- and sphere-organizing regions of the lampbrush chromosomes and secondary constrictions of the mitotic chromosomes
inferredcites →https://doi.org/10.1007/bf01931895openalex-snapshot
Completion of the morphology of the lampbrush chromosomes of the Italian alpine newtTriturus alpestris apuanus bonaparte
inferredcites →https://doi.org/10.1007/bf02136887openalex-snapshot
Chromosomal heteromorphism and female heterogamety in the marbled newtTriturus marmoratus (Latreille, 1800)
inferredcites →https://doi.org/10.1007/bf02142257openalex-snapshot
Synchrone Replikation aller Chromosomen beiXenopus laevis
inferredcites →https://doi.org/10.1007/bf02151711openalex-snapshot
Heterochromosomen beiVipera berus L. (Viperidae, Serpentes)
inferredcites →https://doi.org/10.1007/bf02983075openalex-snapshot
Sex ratio and unisexual sterility in hybrid animals
inferredcites →https://doi.org/10.1016/0014-4827(72)90558-7openalex-snapshot
A simple technique for demonstrating centromeric heterochromatin
inferredcites →https://doi.org/10.1038/hdy.1947.4openalex-snapshot
Colour inheritance and sex determination in Lebistes
inferredcites →https://doi.org/10.1073/pnas.25.5.233openalex-snapshot
Induction of Triploidy and Haploidy in the Newt, Triturus Viridescens, by Cold Treatment of Unsegmented Eggs
inferredcites →https://doi.org/10.1073/pnas.69.3.629openalex-snapshot
Quinacrine, A Chromosome Stain Specific for Deoxyadenylate-Deoxythymidylate-Rich Regions in DNA
inferredcites →https://doi.org/10.1080/00087114.1964.10796130openalex-snapshot
Il Corredo Cromosomico diDiscoglossus PictusOtth: Cromosomi Sessuali, Spiralizzazione Cromosomica e Zone Eterocromatiche
inferredcites →https://doi.org/10.1080/00087114.1965.10796196openalex-snapshot
Le Mappe dei Cromosomi « Lampbrush » diTriturus(Anfibi Urodeli). I.Triturus Alpestris Apuanus
inferredcites →https://doi.org/10.1080/11250007109429162openalex-snapshot
Comparative Karyology of the Amphibia
inferredcites →https://doi.org/10.1086/281274openalex-snapshot
Sex Determination in Triturus vulgaris Linn (Taeniatus Schneid)
inferredcites →https://doi.org/10.1093/genetics/52.3.695openalex-snapshot
THE GENETICS OF ARTEMIA SALINA. V. CROSSING OVER BETWEEN THE X AND Y CHROMOSOMES
inferredcites →https://doi.org/10.1098/rstb.1960.0007openalex-snapshot
Lampbrush chromosomes of crested newts Triturus cristatus (Laurenti)
inferredcites →https://doi.org/10.1101/sqb.1974.038.01.048openalex-snapshot
Fluorescent Probes of Chromosomal DNA Structure: Three Classes of Acridines
inferredcites →https://doi.org/10.1111/j.1601-5223.1940.tb03229.xopenalex-snapshot
TRIPLOIDY IN TRITON TAENIATUS LAUR
inferredcites →https://doi.org/10.1111/j.1601-5223.1945.tb02756.xopenalex-snapshot
CYTOLOGICAL STUDIES ON DIPNOI, URODELA, ANURA, AND EMYS
inferredcites →https://doi.org/10.1126/science.144.3626.1578openalex-snapshot
Amphibian Cell Culture: Permanent Cell Line from the Bullfrog ( Rana catesbeiana )
inferredcites →https://doi.org/10.1139/g78-023openalex-snapshot
SEX CHROMOSOME DIFFERENTIATION: AN INTERMEDIATE STAGE IN A LIZARD
inferredcites →https://doi.org/10.1159/000129731openalex-snapshot
Cytological Confirmation of Female Heterogamety in the African Water Frog (Xenopus laevis)
inferredcites →https://doi.org/10.1159/000129818openalex-snapshot
An Air-Drying Method for Meiotic Preparations from Mammalian Testes
inferredcites →https://doi.org/10.1159/000129880openalex-snapshot
The Mitotic Chromosomes in Xenopus laevis (Daudin): Normal, Sex Reversed and Female WW
inferredcites →https://doi.org/10.1159/000130197openalex-snapshot
Karyotype analysis of Xenopus muelleri (Peters) and Xenopus laevis(Daudin), Pipidae
inferredcites →https://doi.org/10.1159/000130468openalex-snapshot
Karyotype analysis of Xenopus tropicalis Gray, Pipidae
inferredcites →https://doi.org/10.1159/000130761openalex-snapshot
A comparative study of the karyotypes of eight Xenopus species and subspecies possessing a 36-chromosome complement
inferredcites →https://doi.org/10.1242/jcs.3.4.615openalex-snapshot
A radioautographic study of the time course of male meiosis in the newt Triturus vulgaris
inferredcites →https://doi.org/10.3109/10520297109067820openalex-snapshot
Rapid Chromosome and Sex-Chromatin Staining with Pinacyanol
inferredcites →https://doi.org/10.3181/00379727-89-21742openalex-snapshot
Breeding of Sex-reversed Males of Xenopus laevis Daudin.
inferredcites →https://doi.org/10.3181/00379727-93-22688openalex-snapshot
Genic Control and Hormonal Reversal of Sex Differentiation in Xenopus.
inferredcites →https://doi.org/10.7326/0003-4819-68-6-1375_2openalex-snapshot
Sex Chromosomes and Sex-linked Genes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.3755.5.1zenodo-depositor-declared
Description of two new species of Microhyla (Anura: Microhylidae) from Bangladesh
inferred← citeshttps://doi.org/10.5852/ejt.2021.764.1475zenodo-depositor-declared
Head in the clouds: a new dwarf frog species of the Physalaemus signifer clade (Leptodactylidae, Leiuperinae) from the top of the Brazilian Atlantic Forest
inferred← citeshttps://doi.org/10.5852/ejt.2022.847.1991zenodo-depositor-declared
A new species of Odontophrynus (Anura, Odontophrynidae) from the southern portion of the Mantiqueira mountains
inferred← citeshttps://doi.org/10.1002/ar.23123openalex-snapshot
Females Have Larger Ratio of Second‐to‐Fourth Digits Than Males in Four Species of S alamandridae, C audata
inferred← citeshttps://doi.org/10.1002/ece3.9436openalex-snapshot
Postmating isolation and evolutionary relationships among Fejervarya species from Lesser Sunda, Indonesia and other Asian countries revealed by crossing experiments and mtDNA Cytb sequence analyses
inferred← citeshttps://doi.org/10.1002/jez.1402480311openalex-snapshot
Cytology, embryology, and evolution of the developmental arrest syndrome in newts of the genus Triturus (Caudata: Salamandridae)
inferred← citeshttps://doi.org/10.1007/978-1-4615-6974-9_4openalex-snapshot
Neontological Inferences of Evolutionary Pattern and Process in the Salamander Family Plethodontidae
inferred← citeshttps://doi.org/10.1007/978-1-4684-7615-6_21openalex-snapshot
Diversity of Sperm Basic Chromosomal Proteins in the Vertebrates: A Phylogenetic Point of View
inferred← citeshttps://doi.org/10.1007/978-3-0348-7781-7_8openalex-snapshot
Sex chromosomes, sex-linked genes, and sex determination in the vertebrate class Amphibia
inferred← citeshttps://doi.org/10.1007/978-3-642-69150-8_3openalex-snapshot
Evolution of Sex Chromosomes and Heterogametic Systems in Amphibia
inferred← citeshttps://doi.org/10.1007/978-94-010-9163-3_23openalex-snapshot
The evolutionary consequence of major genomic changes in Amphibia
inferred← citeshttps://doi.org/10.1007/bf00056062openalex-snapshot
Chromosome differentiation in the Triturus alpestris complex (Amphibia: Caudata)
inferred← citeshttps://doi.org/10.1007/bf00058671openalex-snapshot
Further evidence for early sex chromosome differentiation of Anuran species
inferred← citeshttps://doi.org/10.1007/bf00120223openalex-snapshot
Chromosomal investigation of three Costa Rican frogs from the 30-chromosome radiation of Hyla with the description of a unique geographic variation in nucleolus organizer regions
inferred← citeshttps://doi.org/10.1007/bf00285826openalex-snapshot
Heterochromatic DNA in Tritmus (Amphibia, Urodela)
inferred← citeshttps://doi.org/10.1007/bf00286030openalex-snapshot
Karyotype evolution and sex chromosome differentiation in schistosomes (Trematoda, Schistosomatidae)
inferred← citeshttps://doi.org/10.1007/bf00286329openalex-snapshot
Cytogenetics of diploid and triploid salamanders of the Ambystoma jeffersonianum complex
inferred← citeshttps://doi.org/10.1007/bf00288674openalex-snapshot
Evolutionary conservation of a common pattern of activity of nucleolus organizers during spermatogenesis in vertebrates
inferred← citeshttps://doi.org/10.1007/bf00292209openalex-snapshot
On the arrangement of chromosomes in the elongated sperm nuclei of Anura (amphibia)
inferred← citeshttps://doi.org/10.1007/bf00292262openalex-snapshot
Cytogenetics of the chinese giant salamander, Andrias davidianus (Blanchard): the evolutionary significance of cryptobranchoid karyotypes
inferred← citeshttps://doi.org/10.1007/bf00292447openalex-snapshot
The evolution of a highly variable sex chromosome in Gehyra purpurascens (Gekkonidae)
inferred← citeshttps://doi.org/10.1007/bf00292789openalex-snapshot
The meiotic structure and behavior of the strongly heteromorphic X/Y sex chromosomes of neotropical plethodontid salamanders of the genus Oedipina
inferred← citeshttps://doi.org/10.1007/bf00292962openalex-snapshot
Heterochromatic DNA in Triturus (Amphibia, Urodela)
inferred← citeshttps://doi.org/10.1007/bf00293412openalex-snapshot
Heteromorphism for chromosome 1, a requirement for normal development in crested newts
inferred← citeshttps://doi.org/10.1007/bf00293837openalex-snapshot
Cytogenetic evolution in the plethodontid salamander genus Aneides
inferred← citeshttps://doi.org/10.1007/bf00294996openalex-snapshot
Chromosome 1 in crested and marbled newts (Triturus)
inferred← citeshttps://doi.org/10.1007/bf00302348openalex-snapshot
An early stage of ZW/ZZ sex chromosome differentiation in Poecilia sphenops var. melanistica (Poeciliidae, Cyprinodontiformes)
inferred← citeshttps://doi.org/10.1007/bf00328638openalex-snapshot
Cytogenetics of the European plethodontid salamanders of the genus Hydromantes (Amphibia, Urodela)
inferred← citeshttps://doi.org/10.1007/bf00329541openalex-snapshot
Evidence for a highly differentiated sex chromosome heteromorphism in the salamander Necturus maculosus (Rafinesque)
inferred← citeshttps://doi.org/10.1007/bf00337599openalex-snapshot
Characterisation of a short, highly repeated and centromerically localised DNA sequence in crested and marbled newts of the genus Triturus
inferred← citeshttps://doi.org/10.1007/bf01175181openalex-snapshot
Sex chromosome associated satellite DNA: Evolution and conservation
inferred← citeshttps://doi.org/10.1007/bf01726693openalex-snapshot
Chromosome banding in Amphibia. XV. Two types of Y chromosomes and heterochromatin hypervariabilty inGastrotheca pseustes (Anura, Hylidae)
inferred← citeshttps://doi.org/10.1007/bf01810826openalex-snapshot
Structural characteristics of genome organization in amphibians: Differential staining of chromosomes and DNA structure
inferred← citeshttps://doi.org/10.1007/bf01955327openalex-snapshot
C-band positive W chromosome in the female Indian frog
inferred← citeshttps://doi.org/10.1007/bf01956473openalex-snapshot
Abnormalities of meioses in male reciprocal hybrids between the Hiroshima and Ichinoseki populations ofRana japonica
inferred← citeshttps://doi.org/10.1007/bf01991633openalex-snapshot
A frog with highly evolved sex chromosomes
inferred← citeshttps://doi.org/10.1007/bf02265048openalex-snapshot
Characterization of DNA sequences constituting the terminal heterochromatin of the chicken Z chromosome
inferred← citeshttps://doi.org/10.1007/bf02424453openalex-snapshot
A comparative study of mitotic and meiotic chromosomes of the Montandon's newt,Triturus montandoni (Urodela: Salamandridae) from Poland and Rumania
inferred← citeshttps://doi.org/10.1007/bf02619666openalex-snapshot
Synergistic effect of TPA and T-cell mitogens in nonmammalian vertebrates
inferred← citeshttps://doi.org/10.1007/s000180050343openalex-snapshot
Amphibian sex determination and sex reversal
inferred← citeshttps://doi.org/10.1007/s00343-019-7320-0openalex-snapshot
Karyological analysis of the sea cicada Blepharipoda liberate Shen from the Rizhao intertidal zone, China
inferred← citeshttps://doi.org/10.1007/s00412-003-0245-5openalex-snapshot
W-derived BAC probes as a new tool for identification of the W chromosome and its aberrations in Bombyx mori
inferred← citeshttps://doi.org/10.1007/s00412-014-0455-zopenalex-snapshot
Sex chromosome polymorphism in guppies
inferred← citeshttps://doi.org/10.1007/s00412-015-0569-yopenalex-snapshot
Dynamics of vertebrate sex chromosome evolution: from equal size to giants and dwarfs
inferred← citeshttps://doi.org/10.1007/s004120050237openalex-snapshot
Evidence for two successive pericentric inversions in sex lampbrush chromosomes of Rana rugosa (Anura: Ranidae)
inferred← citeshttps://doi.org/10.1007/s004120050275openalex-snapshot
Lampbrush chromosomes and chiasmata of sex-reversed crested newts
inferred← citeshttps://doi.org/10.1007/s004120050366openalex-snapshot
Molecular differentiation of sex chromosomes probed by comparative genomic hybridization
inferred← citeshttps://doi.org/10.1007/s10577-007-1139-9openalex-snapshot
Establishment of high-resolution FISH mapping system and its application for molecular cytogenetic characterization of chromosomes in newt, Cynops pyrrhogaster (Urodela, Amphibia)
inferred← citeshttps://doi.org/10.1007/s10577-008-1197-7openalex-snapshot
Cytogenetic analysis of the Asian Plethodontid salamander, Karsenia koreana: Evidence for karyotypic conservation, chromosome repatterning, and genome size evolution
inferred← citeshttps://doi.org/10.1007/s10709-007-9169-yopenalex-snapshot
Molecular phylogeny and karyotype differentiation in Paratelmatobius and Scythrophrys (Anura, Leptodactylidae)
inferred← citeshttps://doi.org/10.1007/s10709-010-9501-9openalex-snapshot
Heteromorphic Z and W sex chromosomes in Physalaemus ephippifer (Steindachner, 1864) (Anura, Leiuperidae)
inferred← citeshttps://doi.org/10.1007/s10709-012-9636-yopenalex-snapshot
Karyotypic differentiation via 2n reduction and a finding of a case of triploidy in anurans of the genus Engystomops (Anura, Leiuperidae)
inferred← citeshttps://doi.org/10.1016/0014-4894(89)90186-0openalex-snapshot
Schistosoma mansoni: Chromosomal localization of DNA repeat elements by in situ hybridization using biotinylated DNA probes
inferred← citeshttps://doi.org/10.1016/0169-5347(91)90088-fopenalex-snapshot
Resolving the phylogeny of the European newts
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50006-8openalex-snapshot
The Phylogeny of Amphibians: Current Knowledge and the Role of Cytogenetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50009-3openalex-snapshot
Evolutionary Cytogenetics of Bolitoglossine Salamanders (Family Plethodontidae)
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50012-3openalex-snapshot
Chromosome Heteromorphism in Newts (Triturus) and Its Significance in Relation to Evolution and Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50017-2openalex-snapshot
Chromosome Evolution in Holarctic Hyla Treefrogs
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50019-6openalex-snapshot
The Evolution of Heterochromatin in the Amphibian Genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-297880-7.50020-2openalex-snapshot
Sex-Determining Mechanisms and Sex Chromosomes in Amphibia
inferred← citeshttps://doi.org/10.1016/b978-0-12-374931-4.10001-xopenalex-snapshot
Sex Determination and Sexual Differentiation in Amphibians
inferred← citeshttps://doi.org/10.1016/b978-0-12-374932-1.00014-7openalex-snapshot
Sex Determination and Sexual Differentiation in Amphibians
inferred← citeshttps://doi.org/10.1016/b978-0-443-16020-2.00012-7openalex-snapshot
Sex determination and gonadal differentiation in amphibians
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.10.018openalex-snapshot
Cytogenetic contributions for the study of the Amazonian Engystomops (Anura; Leiuperidae) assessed in the light of phylogenetic relationships
inferred← citeshttps://doi.org/10.1016/s0022-5193(88)80022-5openalex-snapshot
Meiotic pairing constraints and the activity of sex chromosomes
inferred← citeshttps://doi.org/10.1023/a:1009241528994openalex-snapshot
The ZW Pairs of Two Paleognath Birds From Two Orders Show Transitional Stages of Sex Chromosome Differentiation
inferred← citeshttps://doi.org/10.1023/a:1009253410553openalex-snapshot
Polymorphism of the Nucleolus Organizer Regions (NORs) in Physalaemus Petersi (Amphibia, Anura, Leptodactylidae) Detected by Silver Staining and Fluorescence In Situ Hybridization
inferred← citeshttps://doi.org/10.1023/a:1018485217391openalex-snapshot
Cytogenetics of the genus Leporinus (Pisces, Anostomidae). 1.Karyotype analysis, heterochromatin distribution and sex chromosomes
inferred← citeshttps://doi.org/10.1023/b:gene.0000019926.50310.26openalex-snapshot
Cytogenetics of Hylodes and Crossodactylus Species (Anura, Leptodactylidae) with Comments on Hylodinae/Dendrobatidae Relationships
inferred← citeshttps://doi.org/10.1038/hdy.1983.25openalex-snapshot
Sex chromosome evolution in the polytypic species Pycnogaster cucullata
inferred← citeshttps://doi.org/10.1038/hdy.1987.118openalex-snapshot
Sex differences in chiasma frequency and distribution in natural populations of Eyprepocnemis plorans containing B-chromosomes
inferred← citeshttps://doi.org/10.1038/hdy.1989.82openalex-snapshot
Characterization of heterochromatic regions in two Triturus alpestris subspecies (Urodela: Salamandridae)
inferred← citeshttps://doi.org/10.1046/j.1420-9101.1990.3050329.xopenalex-snapshot
An integrative analysis of phylogenetic relationships among newts of the genus Triturus (family Salamandridae), using comparative biochemistry, cytogenetics and reproductive interactions
inferred← citeshttps://doi.org/10.1080/00087114.1984.10797682openalex-snapshot
Chromosome I and Sex Determination of Crested Newts
inferred← citeshttps://doi.org/10.1080/00087114.1985.10797729openalex-snapshot
Karyotypic Study of Some Species of Family Parodontidae (Pisce—Cypriniformes)
inferred← citeshttps://doi.org/10.1080/00087114.1986.10797801openalex-snapshot
The Meiotic System of Iberian Species of the GenusTriturus(Amphibia: Caudata)
inferred← citeshttps://doi.org/10.1080/00087114.1993.10797275openalex-snapshot
Heterochromatin heterogeneity inTriturus marmoratus(Urodela: Salamandridae) demonstrated with specific DNA-binding fluorochromes and «in situ» restriction endonuclease/nick translation
inferred← citeshttps://doi.org/10.1080/00087114.2000.10589207openalex-snapshot
Cytogenetic analysis of three Physalaemus species (Amphibia, Anura)
inferred← citeshttps://doi.org/10.1080/00785326.1999.10409409openalex-snapshot
The XX-XY (male-heterogametic) sex chromosome system inPolydora curiosa(Polychaeta: Spionidae)
inferred← citeshttps://doi.org/10.1080/11250000309356514openalex-snapshot
Intrageneric karyotypic divergence inScythrophrysand new insights into the relationship withParatelmatobius(Anura, Leptodactylidae)
inferred← citeshttps://doi.org/10.1086/668076openalex-snapshot
The Balanced Lethal System of Crested Newts: A Ghost of Sex Chromosomes Past?
inferred← citeshttps://doi.org/10.1093/biolinnean/blac153openalex-snapshot
Chromosome and bands: comparative cytogenetics of the morphotypes ofAmeerega trivittata(Anura: Dendrobatidae)
inferred← citeshttps://doi.org/10.1093/gbe/evaf155openalex-snapshot
Identification of Y-chromosome Turnover in Newts Fails to Support a Sex Chromosome Origin for the Triturus Balanced Lethal System
inferred← citeshttps://doi.org/10.1098/rspb.2015.2691openalex-snapshot
Meiotic recombination counteracts male-biased mutation (male-driven evolution)
inferred← citeshttps://doi.org/10.1098/rstb.1986.0005openalex-snapshot
The biological significance of variation in satellite DNA and heterochromatin in newts of the genus Triturus : an evolutionary perspective
inferred← citeshttps://doi.org/10.1111/1755-0998.70019openalex-snapshot
Linkage Mapping vs. Association: A Comparison of Two RADseq ‐Based Approaches to Identify Markers for Homomorphic Sex Chromosomes in Large Genomes
inferred← citeshttps://doi.org/10.1111/j.1432-0436.1981.tb01169.xopenalex-snapshot
H-Y Antigen and Sex-Determination in Turtles
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1980.00079.xopenalex-snapshot
CHANGES OF CHROMOSOMES DURING THE EARLY NEURAL DEVELOPMENT OF A JAPANESE NEWT, CYNOPS PYRRHOGASTER
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1990.tb01426.xopenalex-snapshot
THE EVOLUTION OF HETEROMORPHIC SEX CHROMOSOMES
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1987.tb03684.xopenalex-snapshot
A natural hybrid newt, Triturus helveticus×T. vulgaris, from a pond in mid‐Wales
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2000.00201.xopenalex-snapshot
Cytogenetics of two Species of Paratelmatobius (Anura: Leptodactylidae), with Phylogenetic Comments
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2004.01775.xopenalex-snapshot
Conserved karyotypes in the Hyla pulchella species group (Anura, Hylidae)
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2009.02153.xopenalex-snapshot
Chromosome analysis in Pseudopaludicola (Anura, Leiuperidae), with description of sex chromosomes XX/XY in P. saltica
inferred← citeshttps://doi.org/10.1111/j.2007.0018-0661.02026.xopenalex-snapshot
Unusual primitive heteromorphic ZZ/ZW sex chromosomes in Proceratophrys boiei (Anura, Cycloramphidae, Alsodinae), with description of C-Band interpopulational polymorphism
inferred← citeshttps://doi.org/10.1139/z99-014openalex-snapshot
Two karyotypes and heteromorphic sex chromosomes in Physalaemus petersi (Anura, Leptodactylidae)
inferred← citeshttps://doi.org/10.1159/000446882openalex-snapshot
Evidence for Sex Chromosome Turnover in Proteid Salamanders
inferred← citeshttps://doi.org/10.11606/issn.2316-9079.v3i1p43-49openalex-snapshot
Chromosomal characterization of Hyla bischoffi and Hyla guentheri (Anura, Hylidae)
inferred← citeshttps://doi.org/10.1163/156853806778189927openalex-snapshot
Karyotypes of four species of megophryid frogs (Anura: Megophryidae) from Thailand
inferred← citeshttps://doi.org/10.1163/156853806778877103openalex-snapshot
Chromosomal analysis of the leptodactylids Pleurodema diplolistris and Physalaemus nattereri (Amphibia, Anura)
inferred← citeshttps://doi.org/10.1186/s12983-018-0291-8openalex-snapshot
Sex chromosomal dimorphisms narrated by X-chromosome translocation in a spiny frog (Quasipaa boulengeri)
inferred← citeshttps://doi.org/10.1201/b18534-14openalex-snapshot
Cephalic Kidney and Spleen Cell Culture in Antarctic Teleosts
inferred← citeshttps://doi.org/10.13128/acta_herpetol-12658openalex-snapshot
Meiotic behavior of two polyploid species of genus Pleurodema (Anura: Leiuperidae) from central Argentina
inferred← citeshttps://doi.org/10.1508/cytologia.65.359openalex-snapshot
Cytogenetics of Edalorhina perezi(Anura, Leptodactylidae).
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2017-0382openalex-snapshot
Cytogenetics of two hylid frogs from Brazilian Cerrado
inferred← citeshttps://doi.org/10.1590/s1415-47572004000300010openalex-snapshot
Cytogenetics of three Brazilian species of Eleutherodactylus (Anura, Leptodactylidae) with 22 chromosomes and re-analysis of multiple translocations in E. binotatus
inferred← citeshttps://doi.org/10.1590/s1415-47572006000200010openalex-snapshot
B-chromosomes in two Brazilian populations of Dendropsophus nanus (Anura, Hylidae)
inferred← citeshttps://doi.org/10.1643/0045-8511(2003)003[0166:kvitgm]2.0.co;2openalex-snapshot
Karyotypic Variation in the Genus Megaelosia (Anura, Hylodinae) with the First Description of a B-Chromosome in a Leptodactylid Frog
inferred← citeshttps://doi.org/10.1643/ch-10-142openalex-snapshot
Redescription of Physalaemus barrioi (Anura: Leiuperidae)
inferred← citeshttps://doi.org/10.1655/0018-0831(2002)058[0293:caofpf]2.0.co;2openalex-snapshot
CYTOGENETIC ANALYSIS OF FOUR POISON FROGS OF THE EPIPEDOBATES GENUS (ANURA: DENDROBATIDAE)
inferred← citeshttps://doi.org/10.20350/digitalcsic/8873openalex-snapshot
Tritón palmeado – Lissotriton helveticus (Razoumowsky, 1789)
inferred← citeshttps://doi.org/10.2108/0289-0003(1998)15[469:sdipae]2.0.co;2openalex-snapshot
Sex Differences in Polymorphism and Expression of AAT-1 in the Hiroshima Population of Buergeria buergeri (Anura, Rhacophoridae)
inferred← citeshttps://doi.org/10.2108/zsj.14.57openalex-snapshot
Delayed Response of QM- and DA/DAPI-Fluorescence in C-Heterochromatin of the Small Japanese Field Mouse, Apodemus argenteus
inferred← citeshttps://doi.org/10.2108/zsj.24.1197openalex-snapshot
Morphological Divergence, Reproductive Isolating Mechanism, and Molecular Phylogenetic Relationships Among Indonesia, Malaysia, and Japan Populations of the Fejervarya limnocharis Complex (Anura, Ranidae)
inferred← citeshttps://doi.org/10.2108/zsj.28.12openalex-snapshot
Taxonomic Status of Three Types ofFejervarya cancrivorafrom Indonesia and Other Asian Countries Based on Morphological Observations and Crossing Experiments
inferred← citeshttps://doi.org/10.2307/1446293openalex-snapshot
Karyology and Systematics of the Salamander Genus Pseudobranchus (Sirenidae)
inferred← citeshttps://doi.org/10.2478/s11756-011-0048-8openalex-snapshot
Redescription of the karyotype of five species of the family Bufonidae (Amphibia: Anura) from central area of Argentina
inferred← citeshttps://doi.org/10.3897/compcytogen.v10i4.9176openalex-snapshot
Karyological study of Ololygon tripui (Lourenço, Nascimento and Pires, 2009), (Anura, Hylidae) with comments on chromosomal traits among populations
inferred← citeshttps://doi.org/10.4236/oalib.1104212openalex-snapshot
Peripheral Blood Lymphocyte Culture of Rhinella arenarum
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