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Chromosome Disorders

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  • B lymphocyte development, heterogeneity, and function  Academic Article
  • Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing  Academic Article
  • Cytogenetic characterization of B-cell lymphomas from severe combined immunodeficiency disease mice given injections of lymphocytes from Epstein-Barr virus-positive donors  Academic Article
  • Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes  Academic Article
  • Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes  Academic Article
  • Gamma heavy chain disease in man: cDNA sequence supports partial gene deletion model  Academic Article
  • Genetic dissection of the learning/memory gene dunce of Drosophila melanogaster  Academic Article
  • Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach  Academic Article
  • Rescue of a telomere length defect of Nijmegen breakage syndrome cells requires NBS and telomerase catalytic subunit  Academic Article
  • Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort  Academic Article

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