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Chromosome 13

  • Centromere RNA Is a Key Component for the Assembly of Nucleoproteins at the Nucleolus and Centromere

    Centromere RNA Is a Key Component for the Assembly of Nucleoproteins at the Nucleolus and Centromere

  • 4P Duplications

    4P Duplications

  • Chromosome 13 Introduction Chromosome 13 (As Well As Chromosomes 14, 15, 21 and 22) Is an Acrocentric Chromosome. Short Arms Of

    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

    Phenotype-Karyotype Correlation in Patientstrisomic

  • Congenital Heart Disease and Chromossomopathies Detected By

    Congenital Heart Disease and Chromossomopathies Detected By

  • Complete Or Partial Homozygosity of Chromosome 13 in Primary Retinobiastoma'

    Complete Or Partial Homozygosity of Chromosome 13 in Primary Retinobiastoma'

  • The Genomic Landscape of Centromeres in Cancers Anjan K

    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

    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

    Cytogenetic and Molecular Studies of Trisomy 13

  • Satellite DNA at the Centromere Is Dispensable for Segregation Fidelity

    Satellite DNA at the Centromere Is Dispensable for Segregation Fidelity

  • Variability of Human Rdna

    Variability of Human Rdna

  • Chromosome Abnormalities

    Chromosome Abnormalities

  • Receptor Signaling Through Osteoclast-Associated Monocyte

    Receptor Signaling Through Osteoclast-Associated Monocyte

  • Chromosomal Instability Is Associated with Higher Expression of Genes

    Chromosomal Instability Is Associated with Higher Expression of Genes

  • GENE LIST ANTI-CORRELATED Systematic Common Description

    GENE LIST ANTI-CORRELATED Systematic Common Description

  • Examination of Trisomy 13, 18 and 21 Foetal Tissues at Different Gestational Ages Using FISH

    Examination of Trisomy 13, 18 and 21 Foetal Tissues at Different Gestational Ages Using FISH

  • Loss of Heterozygosity on Chromosomes 3, 13, and 17

    Loss of Heterozygosity on Chromosomes 3, 13, and 17

  • Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21

    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


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