Understanding the Evolution of Reptile Chromosomes through Applications of Combined Cytogenetics and Genomics Approaches
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000495974
ZZ/ZW Sex Chromosomes in the Endemic Puerto Rican Leaf-Toed Gecko (Phyllodactylus wirshingi)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496379
Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000498836
Microarray Profiling of Circular RNA Identifies hsa_circ_0126991 as a Potential Risk Factor for Essential Hypertension
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500063
Evolution of Bird Sex Chromosomes Narrated by Repetitive Sequences: Unusual W Chromosome Enlargement in Gallinula melanops (Aves: Gruiformes: Rallidae)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000501381
Male Meiotic Recombination in the Steppe Agama, Trapelus sanguinolentus (Agamidae, Iguania, Reptilia)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496078
The Mobilome of Reptiles: Evolution, Structure, and Function
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496416
Cytogenetic Analysis and Chromosomal Mapping of Repetitive DNA in Melipona Species (Hymenoptera, Meliponini)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000501754
Karyotype Evolution and Distinct Evolutionary History of the W Chromosomes in Swallows (Aves, Passeriformes)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500621
Aberrant Meiotic Configurations Cause Sterility in Clone-Origin Triploid and Inter-Group Hybrid Males of the Dojo Loach, Misgurnus anguillicaudatus
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500303
Karyotype Analysis of Four Blind Snake Species (Reptilia: Squamata: Scolecophidia) and Karyotypic Changes in Serpentes
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496554
Insights into Emydid Turtle Cytogenetics: The European Pond Turtle as a Model Species
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000495833
Population-Based Cytogenetic Banding Analysis and Phylogenetic Relationships of the Neotropical Fungus-Farming Ant Trachymyrmex holmgreni Wheeler, 1925
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503913
Discovery of Putative XX/XY Male Heterogamety in Emydura subglobosa Turtles Exposes a Novel Trajectory of Sex Chromosome Evolution in Emydura
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000501891
Isolating Chromosomes of the Komodo Dragon: New Tools for Comparative Mapping and Sequence Assembly
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496171
Anti-Apoptotic Effects of Docosahexaenoic Acid in IL-1β-Induced Human Chondrosarcoma Cell Death through Involvement of the MAPK Signaling Pathway
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500290
Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000496077
5-Methylcytosine-Rich Heterochromatin in Reptiles
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000495893
Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000499886
Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500735
DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500468
Characterization of VvSPL18 and Its Expression in Response to Exogenous Hormones during Grape Berry Development and Ripening
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503912
Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503267
Comparative Study of the Bush Dog (Speothos venaticus) Karyotype and Analysis of Satellite DNA Sequences and Their Chromosome Distribution in Six Species of Canidae
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503082
Three Novel Aberrations Involving PLAG1 Leading to Lipoblastoma in Three Different Patients: High Amplification, Partial Deletion, and a Unique Complex Rearrangement
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503158
Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000499325
A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500619
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000502598
Chromosomal Evolution in the Amolops mantzorum Species Group (Ranidae; Anura) Narrated by Repetitive DNAs
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000499416
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504238
Phenotypic and Genetic Characteristics of Five Korean Patients with Costello Syndrome
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000502045
Novel and Private EDA Mutations and Clinical Phenotypes of Korean Patients with X-Linked Hypohidrotic Ectodermal Dysplasia
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500214
Epigenetic Coactivation of MAGEA6 and CT-GABRA3 Defines Orientation of a Segmental Duplication in the Human X Chromosome
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000502933
Considerable Synteny and Sequence Similarity of Primate Chromosomal Region VIIq31
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000500796
Identification and Analysis of lncRNAs by Whole-Transcriptome Sequencing in Porcine Preadipocytes Induced by BMP2
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000501182
Two-Generation Transmission of Trisomy 18p: Prenatal Diagnosis in a Woman with Mild Intellectual Disability
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000499173
Regulation of the Sox3 Gene in an X0/X0 Mammal without Sry, the Amami Spiny Rat, Tokudaia osimensis
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504313
Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504159
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504075
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000499640
Contents Vol. 158, 2019
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503240
Molecular Characterization of a Familial 13.6-Mb 20p11.1p12.1 Duplication without Clinical Consequence
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000498904
New Comparative Cytogenetic Data on Three Genera of Armored Catfishes of Ancistrini (Loricariidae: Hypostominae)
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504723
Unbalanced Y;7 Translocation between Two Low-Similarity Sequences Leading to SRY-Positive 45,X Testicular Disorders of Sex Development
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000501378
Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503574
Misdivision of Telocentrics and Isochromosomes in Wheat
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000497301
Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000503266
Chromosomal Microarray Analysis in Taiwanese Patients with Williams-Beuren Syndrome
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000505282
Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504820
Whole-Genome and Segmental Homozygosity Confirm Errors in Meiosis as Etiology of Struma Ovarii
来源期刊:Cytogenetic and Genome ResearchDOI:10.1159/000504908