Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 2
Results: 20
Clustering of haplotypes based on phylogeny: how good a strategy for association testing?
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 202, doi. 10.1038/sj.ejhg.5201501
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Carrier testing in minors: a systematic review of guidelines and position papers.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 133, doi. 10.1038/sj.ejhg.5201509
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Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 253, doi. 10.1038/sj.ejhg.5201510
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Genetics of the Lp(a)/apo(a) system in an autochthonous Black African population from the Gabon.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 190, doi. 10.1038/sj.ejhg.5201512
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Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 151, doi. 10.1038/sj.ejhg.5201526
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Optimal genotype determination in highly multiplexed SNP data.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 207, doi. 10.1038/sj.ejhg.5201528
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Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 222, doi. 10.1038/sj.ejhg.5201529
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Do we need a uniform regulatory system for biobanks across Europe?
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 245, doi. 10.1038/sj.ejhg.5201530
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Recent advances in array comparative genomic hybridization technologies and their applications in human genetics.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 139, doi. 10.1038/sj.ejhg.5201531
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Say what we mean, mean what we say.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 149, doi. 10.1038/sj.ejhg.5201533
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Segmental duplication density decrease with distance to human-mouse breaks of synteny.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 216, doi. 10.1038/sj.ejhg.5201534
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A novel mutation in PAX9 causes familial form of molar oligodontia.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 173, doi. 10.1038/sj.ejhg.5201536
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Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 249, doi. 10.1038/sj.ejhg.5201537
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Sex-specific, male-line transgenerational responses in humans.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 159, doi. 10.1038/sj.ejhg.5201538
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Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 180, doi. 10.1038/sj.ejhg.5201540
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Family based association analysis of the IL2 and IL15 genes in allergic disorders.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 227, doi. 10.1038/sj.ejhg.5201541
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BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 167, doi. 10.1038/sj.ejhg.5201542
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Hidden population substructures in an apparently homogeneous population bias association studies.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 236, doi. 10.1038/sj.ejhg.5201546
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Reply to Dr Martin.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 149, doi. 10.1038/sj.ejhg.5201555
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Epigenetics: Sins of the fathers, and their fathers.
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- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 131, doi. 10.1038/sj.ejhg.5201567
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