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American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.American Journal of Human Genetics|August 1, 1993
Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defectC M Howard, G E Davies, M J Farrer, et al.American Journal of Human Genetics|September 1, 1993
COII/tRNA(Lys) intergenic 9-bp deletion and other mtDNA markers clearly reveal that the Tharus (southern Nepal) have Oriental affinitiesG Passarino, O Semino, G Modiano, et al.American Journal of Human Genetics|September 1, 1993
Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosisN Moghrabi, D J Clarke, B Burchell, et al.American Journal of Human Genetics|October 1, 1993
Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplicationC A Wise, C A Garcia, S N Davis, et al.American Journal of Human Genetics|October 1, 1993
Identification of repeat sequence heterogeneity at the polymorphic short tandem repeat locus HUMTH01[AATG]n and reassignment of alleles in population analysis by using a locus-specific allelic ladderC Puers, H A Hammond, L Jin, et al.American Journal of Human Genetics|November 1, 1993
High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in TunisiaC Nishigori, M Zghal, T Yagi, et al.American Journal of Human Genetics|November 1, 1993
Testing independence of fragment lengths within VNTR lociS Geisser, W JohnsonAmerican Journal of Human Genetics|November 1, 1993
Independence tests for VNTR alleles defined as quantile binsB S WeirPageof 980