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American Journal of Human Genetics|March 1, 1996
FMR1 in global populationsC B Kunst, C Zerylnick, L Karickhoff, et al.American Journal of Human Genetics|April 1, 1996
Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in CaucasiansH L Tai, E Y Krynetski, C R Yates, et al.American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.American Journal of Human Genetics|April 1, 1996
Cystic fibrosis heterozygote screening in 5,161 pregnant womenD R Witt, C Schaefer, P Hallam, et al.American Journal of Human Genetics|April 1, 1996
Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerationsN J Risch, H ZhangAmerican Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.American Journal of Human Genetics|June 1, 1993
Phenotype/genotype correlations in Gaucher disease type I: clinical and therapeutic implicationsA Sibille, C M Eng, S J Kim, et al.American Journal of Human Genetics|June 1, 1993
Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14S E Antonarakis, J L Blouin, J Maher, et al.American Journal of Human Genetics|June 1, 1993
Negative expansion of the myotonic dystrophy unstable sequenceD Abeliovich, I Lerer, I Pashut-Lavon, et al.American Journal of Human Genetics|December 1, 1995
Human beta-globin gene polymorphisms characterized in DNA extracted from ancient bones 12,000 years oldE Béraud-Colomb, R Roubin, J Martin, et al.Pageof 979