Works matching IS 10184813 AND DT 2000 AND VI 8 AND IP 10
Results: 16
Inferring the impact of linguistic boundaries on population differentiation: application to the Afro-Asiatic–Indo-European case.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 750, doi. 10.1038/sj.ejhg.5200519
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- Article
Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 801, doi. 10.1038/sj.ejhg.5200525
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- Article
Inheritance of human longevity in Iceland.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 743, doi. 10.1038/sj.ejhg.5200527
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- Article
Hereditary spastic paraplegia caused by mutations in the SPG4 gene.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 771, doi. 10.1038/sj.ejhg.5200528
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- Article
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 757, doi. 10.1038/sj.ejhg.5200529
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- Article
Protection of privacy by third-party encryption in genetic research in Iceland.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 739, doi. 10.1038/sj.ejhg.5200530
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A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 805, doi. 10.1038/sj.ejhg.5200531
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Psychological consequences of predictive genetic testing: a systematic review.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 731, doi. 10.1038/sj.ejhg.5200532
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From developmental biology to dysmorphology.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 813, doi. 10.1038/sj.ejhg.5200534
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Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 793, doi. 10.1038/sj.ejhg.5200535
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FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 764, doi. 10.1038/sj.ejhg.5200536
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NRL S50T mutation and the importance of ‘founder effects’ in inherited retinal dystrophies.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 783, doi. 10.1038/sj.ejhg.5200538
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A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 797, doi. 10.1038/sj.ejhg.5200540
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The IL9R region contribution in asthma is supported by genetic association in an isolated population.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 788, doi. 10.1038/sj.ejhg.5200541
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- Article
A refined physical and transcriptional map of the SPG9 locus on 10q23.3–q24.2.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 777, doi. 10.1038/sj.ejhg.5200546
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Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 809, doi. 10.1038/sj.ejhg.5200547
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