Works matching IS 10184813 AND DT 2001 AND VI 9 AND IP 5
Results: 12
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 319, doi. 10.1038/sj.ejhg.5200591
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- Article
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 328, doi. 10.1038/sj.ejhg.5200626
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- Article
High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 364, doi. 10.1038/sj.ejhg.5200627
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- Article
Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 375, doi. 10.1038/sj.ejhg.5200628
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- Article
Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 388, doi. 10.1038/sj.ejhg.5200632
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- Article
Analytic power calculation for QTL linkage analysis of small pedigrees.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 335, doi. 10.1038/sj.ejhg.5200634
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- Article
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 355, doi. 10.1038/sj.ejhg.5200635
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- Article
Association between quantitative traits underlying asthma and the HLA-DRB1 locus in a family-based population sample.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 341, doi. 10.1038/sj.ejhg.5200636
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- Article
A personal view on reviewing the psychological consequences of predictive genetic testing for late onset disease.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 392, doi. 10.1038/sj.ejhg.5200637
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- Article
Reply to letter from G Evers-Kiebooms.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 393, doi. 10.1038/sj.ejhg.5200638
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- Article
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200640
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- Article
Genetic polymorphism of MUC7: Allele frequencies and association with asthma.
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- European Journal of Human Genetics, 2001, v. 9, n. 5, p. 347, doi. 10.1038/sj.ejhg.5200642
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- Article