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Chromosome 13
Centromere RNA Is a Key Component for the Assembly of Nucleoproteins at the Nucleolus and Centromere
4P Duplications
Chromosome 13 Introduction Chromosome 13 (As Well As Chromosomes 14, 15, 21 and 22) Is an Acrocentric Chromosome. Short Arms Of
Phenotype-Karyotype Correlation in Patientstrisomic
Congenital Heart Disease and Chromossomopathies Detected By
Complete Or Partial Homozygosity of Chromosome 13 in Primary Retinobiastoma'
The Genomic Landscape of Centromeres in Cancers Anjan K
Allele-Specific Disparity in Breast Cancer Fatemeh Kaveh1, Hege Edvardsen1, Anne-Lise Børresen-Dale1,2, Vessela N Kristensen1,2,3* and Hiroko K Solvang1,4
Cytogenetic and Molecular Studies of Trisomy 13
Satellite DNA at the Centromere Is Dispensable for Segregation Fidelity
Variability of Human Rdna
Chromosome Abnormalities
Receptor Signaling Through Osteoclast-Associated Monocyte
Chromosomal Instability Is Associated with Higher Expression of Genes
GENE LIST ANTI-CORRELATED Systematic Common Description
Examination of Trisomy 13, 18 and 21 Foetal Tissues at Different Gestational Ages Using FISH
Loss of Heterozygosity on Chromosomes 3, 13, and 17
Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
Top View
FIRST TRIMESTER SCREENING for DOWN SYNDROME and TRISOMIES 13 & 18 Maternal Serum Screening & Nuchal Translucency/Nasal Bone Sonogram
Mitochondrial Ribosomal Proteins: Candidate Genes for Mitochondrial Disease James E
Evolution of the Human Chromosome 13 Synteny: Evolutionary Rearrangements, Plasticity, Human Disease Genes and Cancer Breakpoints
Chromosome 13
Centromere Deletion in Cryptococcus Deuterogattii Leads to Neocentromere Formation and Chromosome Fusions Klaas Schotanus, Joseph Heitman*
A Database of Fragile Sites in Human Chromosomes
A Case of Mosaic Ring Chromosome 13 Syndrome
Basic Principles of Human Genetics: a Primer for Oral Medicine Harold C
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Trisomy 13 — Patau Syndrome
Human Chromosome 18 and Acrocentrics: a Dangerous Liaison
Nuclear-Mitochondrial DNA Segments Resemble Paternally Inherited Mitochondrial DNA in Humans
Case Report Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
NIPT Fact Sheet
Immunolocalization of CENP-A Suggests a Distinct Nucleosome Structure at the Inner Kinetochore Plate of Active Centromeres Peter E
Trisomy 13 – Patau Syndrome
Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
The Complete Sequence of a Human Genome
An Integrated Genetic Map of the Pearl Locus of Mouse Chromosome 13 Albert B
Table S1. Diseases and Disorders Associated with Structural And/Or Molecular Abnormalities of Chromosome 13
Ring 13 FTNW
Identification of Two Distinct Deleted Regions on Chromosome 13 In
The Chromosome 13 Conundrum in Multiple Myeloma Brian A
Mitochondrial Genomes of Columbicola Feather Lice Are Highly Fragmented, Indicating Repeated Evolution of Minicircle-Type Genomes in Parasitic Lice
Molecular Characterization of a Complex Small Supernumerary Marker Chromosome Derived from Chromosome 18P: an Addition to the Li
Centromere Scission Drives Chromosome Shuffling and Reproductive Isolation
Outcome Following Autosomal Monosomy and Multiple Aneuploidy Results by Noninvasive Prenatal Screening
Duplications of 10P FTNW
Humcfs: a Database of Fragile Sites in Human Chromosomes
What Is a Centromere?
The DNA Sequence and Analysis of Human Chromosome 13
REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
Subsequent Trisomy 13 Pregnancies of Parents with Normal Karyotype
Chromosome Analysisanalysis Nationalnational DNADNA Dayday Aprilapril 25,25, 20052005