Showing results (1361-1370 of 9,790) with videos related to

Sort By:
Pageof 979
American Journal of Human Genetics|August 26, 2000
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutationsP A Isotalo, G A Wells, J G Donnelly
American Journal of Human Genetics|August 26, 2000
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degenerationA Rivera, K White, H Stöhr, et al.
American Journal of Human Genetics|September 1, 2000
Transmission/disequilibrium tests using multiple tightly linked markersH Zhao, S Zhang, K R Merikangas, et al.
American Journal of Human Genetics|September 1, 2000
Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15qL N Bull, E Roche, E J Song, et al.
American Journal of Human Genetics|September 23, 2000
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15G Stöber, K Saar, F Rüschendorf, et al.
American Journal of Human Genetics|September 23, 2000
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.
American Journal of Human Genetics|April 14, 2000
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brainR L Touraine, T Attié-Bitach, E Manceau, et al.
American Journal of Human Genetics|July 6, 2000
Localization of multiple melanoma tumor-suppressor genes on chromosome 11 by use of homozygosity mapping-of-deletions analysisE K Goldberg, J M Glendening, Z Karanjawala, et al.
American Journal of Human Genetics|July 25, 2000
Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II geneZ Deng, J H Morse, S L Slager, et al.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Pageof 979