Works matching IS 10184813 AND DT 2003 AND VI 11 AND IP 3
Results: 11
Reduced folate carrier polymorphism (80A?G) and neural tube defects.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 245, doi. 10.1038/sj.ejhg.5200946
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Finnish and Swedish genotypes and risk of cancer in Sweden.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 207, doi. 10.1038/sj.ejhg.5200947
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Italian family with two independent mutations: 3358T/A in BRCA1 and 8756delA in BRCA2 genes.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 210, doi. 10.1038/sj.ejhg.5200948
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- Article
Mitochondrial DNA analysis reveals diverse histories of tribal populations from India.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 253, doi. 10.1038/sj.ejhg.5200949
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- Article
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 265, doi. 10.1038/sj.ejhg.5200950
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Microsatellite marker association at chromosome region 2p13 in Finnish patients with preeclampsia and obstetric cholestasis suggests a common risk locus.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 232, doi. 10.1038/sj.ejhg.5200951
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Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 271, doi. 10.1038/sj.ejhg.5200952
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ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 215, doi. 10.1038/sj.ejhg.5200953
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Association of NOD2 with Crohn's Disease in a homogenous Irish population.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 237, doi. 10.1038/sj.ejhg.5200954
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A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 225, doi. 10.1038/sj.ejhg.5200955
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- Article
Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1.
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- European Journal of Human Genetics, 2003, v. 11, n. 3, p. 275, doi. 10.1038/sj.ejhg.5200957
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- Article