DOCSLIB.ORG
  • Sign Up
  • Log In
  • Upload
  • Sign Up
  • Log In
  • Upload
  • Home
  • »  Tags
  • »  Chromosome 15

Chromosome 15

  • Impact of Fluorescence in Situ Hybridization in the Detection of Cryptic Fusion Transcript PML/RARA and a Complex T(5;15;17) in a Case of Acute Promyelocytic Leukemia

    Impact of Fluorescence in Situ Hybridization in the Detection of Cryptic Fusion Transcript PML/RARA and a Complex T(5;15;17) in a Case of Acute Promyelocytic Leukemia

  • Rapid Molecular Assays to Study Human Centromere Genomics

    Rapid Molecular Assays to Study Human Centromere Genomics

  • Chromosome Translocation, Recombination, and Nondisjunction

    Chromosome Translocation, Recombination, and Nondisjunction

  • Functional Epialleles at an Endogenous Human Centromere

    Functional Epialleles at an Endogenous Human Centromere

  • 15 Chromosome Chapter

    15 Chromosome Chapter

  • Chromosomal Disorders

    Chromosomal Disorders

  • Rare Allelic Forms of PRDM9 Associated with Childhood Leukemogenesis

    Rare Allelic Forms of PRDM9 Associated with Childhood Leukemogenesis

  • With Acute Promyelocytic Leukemia (Somatic Cell Hybrids/C-Fes/Localization of Breakpoints/Gene Mapping) DENISE SHEER*, LYNNE R

    With Acute Promyelocytic Leukemia (Somatic Cell Hybrids/C-Fes/Localization of Breakpoints/Gene Mapping) DENISE SHEER*, LYNNE R

  • 15Q26 Deletions FTNW

    15Q26 Deletions FTNW

  • Receptor Signaling Through Osteoclast-Associated Monocyte

    Receptor Signaling Through Osteoclast-Associated Monocyte

  • Rarechromo.Org

    Rarechromo.Org

  • (12) Patent Application Publication (10) Pub. No.: US 2011/0196614 A1 Banchereau Et Al

    (12) Patent Application Publication (10) Pub. No.: US 2011/0196614 A1 Banchereau Et Al

  • Genomic Structure of Murine Mitochondrial DNA Polymerase- Gamma

    Genomic Structure of Murine Mitochondrial DNA Polymerase- Gamma

  • Recurrent Rearrangements in the Proximal 15Q11–Q14 Region: a New Breakpoint Cluster Specific to Unbalanced Translocations

    Recurrent Rearrangements in the Proximal 15Q11–Q14 Region: a New Breakpoint Cluster Specific to Unbalanced Translocations

  • Alpha Satellite DNA Biology: Finding Function in the Recesses of the Genome

    Alpha Satellite DNA Biology: Finding Function in the Recesses of the Genome

  • Uniparental Disomy Chromosome 15

    Uniparental Disomy Chromosome 15

  • Chromosome 15 Abnormalities and the Prader-Willi Syndrome: a Follow-Up Report of 40 Cases

    Chromosome 15 Abnormalities and the Prader-Willi Syndrome: a Follow-Up Report of 40 Cases

  • Translocations Involving the Short Arm of Chromosome 17 in Chronic B-Lymphoid Disorders

    Translocations Involving the Short Arm of Chromosome 17 in Chronic B-Lymphoid Disorders

Top View
  • Distribution of the D15Z1 Copy Number Polymorphism
  • The Prader-Willi Syndrome and Interstitial Deletion of Chromosome 15
  • Handbook on Genetics
  • Illustrations Depicting Chromosome 15 and the UBE3A Gene
  • 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
  • Prader-Willi Syndrome
  • Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
  • Tetrasomy 15Q26: a Distinct Syndrome Or Shprintzen-Goldberg Syndrome Phenocopy?
  • Chromosome 15 Structural Abnormalities: Effect on IGF1R Gene Expression and Function
  • 15Q13.3 Microdeletion
  • Rare Autosomal Trisomy & NIPT
  • Chromosome 15 in Floppy Infants Copyright
  • 15Q Deletions FTNW
  • ISOCHROMOSOME NEOCENTROMERE 15Qter MOSAICISM Siri Huston, Yvette Rush, Tom Hempel, Ann Olney, Hope Chipman and Warren G
  • Supplemental Table 1
  • Genome-Wide Linkage Analysis of Gene Expression of Loin Muscle Tissue Identifies Candidate Genes in Pigs
  • Supernumerary Marker of Chromosome 15 Associated With


© 2024 Docslib.org    Feedback