Works matching IS 00034800 AND DT 1999 AND VI 63 AND IP 1
Results: 6
Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 9
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- Article
Relative efficiencies of the Chi-square recombination models for gene mapping with human pedigree data.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 81
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- Article
Evolution of the apolipoprotein B gene and coronary artery disease: a study in low and high risk Asians.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 45
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- Article
Locus and population specific evolution in HLA class II genes.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 27
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- Article
Combined segregation and linkage analysis of nonsyndromic orofacial cleft in two candidate regions.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 17
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- Article
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
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- Annals of Human Genetics, 1999, v. 63, n. 1, p. 1
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- Article