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American Journal of Human Genetics|November 20, 2002
RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibilityChristina G S Palmer, Joni A Turunen, Janet S Sinsheimer, et al.American Journal of Human Genetics|October 2, 2002
Genomewide linkage analysis of body mass index across 28 years of the Framingham Heart StudyLarry D Atwood, Nancy L Heard-Costa, L Adrienne Cupples, et al.American Journal of Human Genetics|June 22, 2002
Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsiaSusanne Kohl, Britta Baumann, Thomas Rosenberg, et al.American Journal of Human Genetics|June 18, 2002
Atypical 5' splice sites cause CFTR exon 9 to be vulnerable to skippingTimothy W Hefferon, Fiona C Broackes-Carter, Ann Harris, et al.American Journal of Human Genetics|June 21, 2002
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/CGiuseppe Novelli, Antoine Muchir, Federica Sangiuolo, et al.American Journal of Human Genetics|June 26, 2002
Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringiaOlga A Derbeneva, Rem I Sukernik, Natalia V Volodko, et al.American Journal of Human Genetics|November 1, 1975
Liver alcohol dehydrogenase in Japanese: high population frequency of atypical form and its possible role in alcohol sensitivityG Stamatoyannopoulos, S H Chen, M FukuiAmerican Journal of Human Genetics|June 12, 2002
Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocationSabrina Giglio, Vladimiro Calvari, Giuliana Gregato, et al.American Journal of Human Genetics|June 12, 2002
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutationsNathan Pankratz, William C Nichols, Sean K Uniacke, et al.American Journal of Human Genetics|March 7, 2003
Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3Carlos Cardoso, Richard J Leventer, Heather L Ward, et al.Pageof 979