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American Journal of Human Genetics|March 31, 2000
Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twinsJ B Whitfield, L M Cullen, E C Jazwinska, et al.
American Journal of Human Genetics|March 31, 2000
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage dataJ A Douglas, M Boehnke, K Lange
American Journal of Human Genetics|March 31, 2000
Segregation analysis in Shwachman-Diamond syndrome: evidence for recessive inheritanceH Ginzberg, J Shin, L Ellis, et al.
American Journal of Human Genetics|March 31, 2000
Surnames and the Y chromosomeB Sykes, C Irven
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
American Journal of Human Genetics|March 31, 2000
A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindredF M Häfner, A A Salam, T E Linder, et al.
American Journal of Human Genetics|March 31, 2000
Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13F Zara, E Gennaro, M Stabile, et al.
American Journal of Human Genetics|March 31, 2000
Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortionsB Lomax, S Tang, E Separovic, et al.
American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.
American Journal of Human Genetics|May 5, 2000
Null alleles of the COL5A1 gene of type V collagen are a cause of the classical forms of Ehlers-Danlos syndrome (types I and II)U Schwarze, M Atkinson, G G Hoffman, et al.
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