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Advanced Drug Delivery Reviews|June 25, 2023
Towards artificial intelligence-enabled extracellular vesicle precision drug deliveryZachary F Greenberg, Kiley S Graim, Mei HeAmerican Journal of Medical Genetics|September 15, 1993
Williams syndrome: autosomal dominant inheritanceC A Morris, I T Thomas, F GreenbergAmerican Journal of Obstetrics and Gynecology|March 1, 1983
Estimates of birth prevalence rates of spina bifida in the United States from computer-generated mapsF Greenberg, L M James, G P OakleyPediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.American Journal of Medical Genetics|April 17, 2001
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African AfrikanersI Simonic, D R Nyholt, G S Gericke, et al.Genome Research|June 1, 1997
Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human regionS Hirotsune, S D Pack, S S Chong, et al.American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.American Journal of Human Genetics|April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17P I Patel, B Franco, C Garcia, et al.Biochimica Et Biophysica Acta|March 20, 2014
Bcl-2 regulation of the inositol 1,4,5-trisphosphate receptor and calcium signaling in normal and malignant lymphocytes: potential new target for cancer treatmentEdward F Greenberg, Andrew R Lavik, Clark W DistelhorstPageof 33