Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 9
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 1999 AND VI 63 AND IP 1
Results: 6
1
2
Locus and population specific evolution in HLA class II genes.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 27
- By:
- Publication type:
- Article
3
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.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 1
- By:
- Publication type:
- Article
4
Relative efficiencies of the Chi-square recombination models for gene mapping with human pedigree data.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 81
- By:
- Publication type:
- Article
5
Evolution of the apolipoprotein B gene and coronary artery disease: a study in low and high risk Asians.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 45
- By:
- Publication type:
- Article
6
Combined segregation and linkage analysis of nonsyndromic orofacial cleft in two candidate regions.
- Published in:
- Annals of Human Genetics, 1999, v. 63, n. 1, p. 17
- By:
- Publication type:
- Article