Works matching IS 10184813 AND DT 2003 AND VI 11 AND IP 8
Results: 14
Computer-based recognition of dysmorphic faces.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 555, doi. 10.1038/sj.ejhg.5200997
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- Article
Genetic information and life insurance: a ‘real’ risk?
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 561, doi. 10.1038/sj.ejhg.5200998
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- Article
Manic depressive illness in a founder population.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 597, doi. 10.1038/sj.ejhg.5201001
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- Article
Comment on ‘CFTR gene mutations in sarcoidosis’.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 553, doi. 10.1038/sj.ejhg.5201003
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- Article
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 623, doi. 10.1038/sj.ejhg.5201005
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- Article
Medical and lay attitudes towards genetic screening and testing in Finland.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 565, doi. 10.1038/sj.ejhg.5201006
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- Article
Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 573, doi. 10.1038/sj.ejhg.5201008
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- Article
Possible consequences of applying guidelines to healthy women with a family history of breast cancer.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 633, doi. 10.1038/sj.ejhg.5201021
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- Article
Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 585, doi. 10.1038/sj.ejhg.5201009
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Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 590, doi. 10.1038/sj.ejhg.5201014
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- Article
Promoter polymorphism influences the effect of dexamethasone on transcriptional activation of the LTC<sub>4</sub> synthase gene.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 619, doi. 10.1038/sj.ejhg.5201015
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- Article
SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 629, doi. 10.1038/sj.ejhg.5201018
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- Article
Genetic variation at the human tissue-type plasminogen activator (tPA) locus: haplotypes and analysis of association to plasma levels of tPA.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 603, doi. 10.1038/sj.ejhg.5201011
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- Article
Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 611, doi. 10.1038/sj.ejhg.5201012
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- Article