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American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.American Journal of Human Genetics|January 23, 1999
Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypesM Tassabehji, K Metcalfe, A Karmiloff-Smith, et al.American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.American Journal of Human Genetics|January 23, 1999
Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneityR Dufourcq-Lagelouse, N Jabado, F Le Deist, et al.American Journal of Human Genetics|January 23, 1999
Hereditary isolated renal magnesium loss maps to chromosome 11q23I C Meij, K Saar, L P van den Heuvel, et al.American Journal of Human Genetics|January 23, 1999
The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPsV Macaulay, M Richards, E Hickey, et al.American Journal of Human Genetics|August 1, 1996
Cost comparison of molecular versus conventional screening of relatives at risk for retinoblastomaH Z Noorani, H N Khan, B L Gallie, et al.American Journal of Human Genetics|August 1, 1996
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of diseaseM H Ruttledge, A A Andermann, C M Phelan, et al.American Journal of Human Genetics|August 1, 1996
Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXEP S Subramanian, D L Nelson, A C ChinaultAmerican Journal of Human Genetics|August 1, 1996
Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyP Benlian, L Foubert, E Gagné, et al.Pageof 979