Showing results (11-20 of 1,615) with videos related to
Sort By:
Pageof 162
American Journal of Human Genetics|March 21, 2000
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3C L Bennett, R Yoshioka, H Kiyosawa, et al.Annals of Human Genetics|July 1, 1978
Characteristics of simple sibship variance tests for the detection of major loci and application to height, weight and spatial performanceP R FainCytogenetics and Cell Genetics|January 1, 1992
Third International Workshop on Human Chromosome 17 MappingP R FainJournal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.Genetic Epidemiology|January 1, 1996
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotypeD F Barker, E R Almeida, G Casey, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.Human Mutation|October 3, 2000
Direct genomic multiplex PCR for BRCA1 and application to mutation detection by single-strand conformation and heteroduplex analysisD F BarkerThe Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.American Journal of Human Genetics|July 1, 1988
Models of multilocus recombination: nonrandomness in chiasma number and crossover positionsD E Goldgar, P R FainPageof 162