Showing results (731-740 of 9,786) with videos related to
Sort By:
Pageof 979
American Journal of Human Genetics|January 1, 1997
Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardationA C Wong, Y Ning, J Flint, et al.American Journal of Human Genetics|January 1, 1997
Fine mapping of the nail-patella syndrome locus at 9q34I McIntosh, M V Clough, A A Schäffer, et al.American Journal of Human Genetics|January 1, 1997
Genetic and environmental architecture of the features of the insulin-resistance syndromeY Hong, N L Pedersen, K Brismar, et al.American Journal of Human Genetics|January 1, 1997
Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophyF Quan, J Janas, S Toth-Fejel, et al.American Journal of Human Genetics|January 1, 1997
Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene GroupR A Norman, D B Thompson, T Foroud, et al.American Journal of Human Genetics|May 1, 1996
An ancient common origin of aboriginal Australians and New Guinea highlanders is supported by alpha-globin haplotype analysisJ M Roberts-Thomson, J J Martinson, J T Norwich, et al.American Journal of Human Genetics|May 1, 1996
Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic neviA M Goldstein, L R Goldin, N C Dracopoli, et al.American Journal of Human Genetics|May 1, 1996
The problem of ascertainment for linkage analysisV J Vieland, S E HodgeAmerican Journal of Human Genetics|May 1, 1996
A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United KingdomS J Knight, R J Ritchie, L Chakrabarti, et al.American Journal of Human Genetics|May 1, 1996
Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiencyS Tomatsu, S Fukuda, A Yamagishi, et al.Pageof 979