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The American Journal of the Medical Sciences|September 1, 1993
Molecular basis of Charcot-Marie-Tooth disease type 1A: gene dosage as a novel mechanism for a common autosomal dominant conditionB B Roa, J R LupskiCurrent Opinion in Obstetrics & Gynecology|April 29, 1998
Applied molecular genetic techniques for prenatal diagnosisI B Van den Veyver, B B RoaGenetic Testing|August 28, 1999
Ashkenazi Jewish population frequency of the Bloom syndrome gene 2281 delta 6ins7 mutationB B Roa, C V Savino, C S RichardsJournal of Bacteriology|September 1, 1989
Overlap between pdxA and ksgA in the complex pdxA-ksgA-apaG-apaH operon of Escherichia coli K-12B B Roa, D M Connolly, M E WinklerJournal of Bacteriology|November 1, 1989
Divergent transcription of pdxB and homology between the pdxB and serA gene products in Escherichia coli K-12P V Schoenlein, B B Roa, M E WinklerInternational Journal of Neurology|January 1, 1991
Charcot-Marie-Tooth disease type 1A: molecular mechanisms of gene dosage and point mutation underlying a common inherited peripheral neuropathyB B Roa, C A Garcia, J R LupskiNature Genetics|October 1, 1996
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2B B Roa, A A Boyd, K Volcik, et al.American Journal of Medical Genetics. Part A|August 13, 2005
Juvenile onset Huntington disease resulting from a very large maternal expansionF A Nahhas, J Garbern, K M Krajewski, et al.Nature Genetics|November 1, 1993
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneB B Roa, P J Dyck, H G Marks, et al.American Journal of Obstetrics and Gynecology|June 16, 2001
Angiotensinogen and endothelial nitric oxide synthase gene polymorphisms among Hispanic patients with preeclampsiaM T Bashford, L A Hefler, T W Vertrees, et al.Pageof 3