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American Journal of Human Genetics|December 1, 1999
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneityK Saar, L Al-Gazali, L Sztriha, et al.
American Journal of Human Genetics|March 7, 2001
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangementsS Giglio, K W Broman, N Matsumoto, et al.
American Journal of Human Genetics|March 7, 2001
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)C Guichard, M C Harricane, J J Lafitte, et al.
American Journal of Human Genetics|February 17, 2001
Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphismsW S Watkins, C E Ricker, M J Bamshad, et al.
American Journal of Human Genetics|February 17, 2001
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2S Guida, F Trettel, S Pagnutti, et al.
American Journal of Human Genetics|February 17, 2001
A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13L M Downey, T J Keen, E Roberts, et al.
American Journal of Human Genetics|February 17, 2001
Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancerC H Bock, J M Cunningham, S K McDonnell, et al.
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