Works matching IS 10184813 AND DT 2001 AND VI 9 AND IP 6
Results: 12
Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 445, doi. 10.1038/sj.ejhg.5200643
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- Article
Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 464, doi. 10.1038/sj.ejhg.5200644
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- Article
Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 452, doi. 10.1038/sj.ejhg.5200645
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- Article
Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1).
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 469, doi. 10.1038/sj.ejhg.5200646
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- Article
Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 409, doi. 10.1038/sj.ejhg.5200649
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- Article
Novel RET mutations in Hirschsprung's disease patients from the diverse South African population.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 419, doi. 10.1038/sj.ejhg.5200650
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- Article
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 437, doi. 10.1038/sj.ejhg.5200651
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BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 424, doi. 10.1038/sj.ejhg.5200652
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Linkage analysis in multiple sclerosis of chromosomal regions syntenic to experimental autoimmune disease loci.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 458, doi. 10.1038/sj.ejhg.5200653
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Meiotic segregation analysis in a t(4;8) carrier: comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 395, doi. 10.1038/sj.ejhg.5200654
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Evaluation of first trimester maternal serum and ultrasound screening for Down's syndrome in Eastern and Northern Finland.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 404, doi. 10.1038/sj.ejhg.5200655
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- Article
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world.
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- European Journal of Human Genetics, 2001, v. 9, n. 6, p. 431, doi. 10.1038/sj.ejhg.5200656
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- Article