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Lancet (London, England)|September 4, 1993
Wolfram syndrome: a mitochondrial-mediated disorder?X Bu, J I RotterClinical Genetics|September 1, 1992
Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locusX Bu, J I RotterGenetic Epidemiology|January 1, 1993
A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysisX Bu, M Shohat, L Jaber, et al.Genetic Epidemiology|January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disordersX Bu, H Y Yang, M Shohat, et al.American Journal of Medical Genetics|September 1, 1992
Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab communityL Jaber, P Merlob, X Bu, et al.American Journal of Human Genetics|January 1, 1995
Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locusC A DeMeester, X Bu, R J Gray, et al.American Journal of Medical Genetics|January 30, 1995
Arthrogryposis multiplex congenita in an Arab kindred: updateL Jaber, R Weitz, X Bu, et al.Journal of Medical Genetics|February 1, 1992
Sensorineural deafness inherited as a tissue specific mitochondrial disorderL Jaber, M Shohat, X Bu, et al.American Journal of Medical Genetics|July 1, 1993
Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13N Fischel-Ghodsian, X Bu, T R Prezant, et al.American Journal of Human Genetics|November 1, 1981
The modes of inheritance of insulin-dependent diabetes mellitus or the genetics of IDDM, no longer a nightmare but still a headacheJ I RotterPageof 25