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Chromosomes, Human, Pair 13

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  • A genome-wide scan for loci linked to forearm bone mineral density  Academic Article
  • A missense mutation of the endothelin-b receptor gene in multigenic hirschsprungs-disease  Academic Article
  • A radiation hybrid map of 95-stss spanning human-chromosome 13q  Academic Article
  • A somatic-cell hybrid map of human-chromosome-13  Academic Article
  • Band-specific localization of the microsatellite at d13s71 by microdissection and enzymatic amplification  Academic Article
  • Chromatin insulator elements block transgene silencing in engineered human embryonic stem cell lines at a defined chromosome 13 locus  Academic Article
  • Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing  Academic Article
  • Cloning and characterization of two human G protein-coupled receptor genes (GPR38 and GPR39) related to the growth hormone secretagogue and neurotensin receptors  Academic Article
  • Identity-by-descent and association mapping of a recessive gene for hirschsprung disease on human-chromosome 13q22  Academic Article
  • Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder  Academic Article
  • Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series  Academic Article
  • Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach  Academic Article
  • Receptor for motilin identified in the human gastrointestinal system  Academic Article
  • Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort  Academic Article
  • The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke  Academic Article

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