Works matching IS 10184813 AND DT 2004 AND VI 12 AND IP 10
Results: 14
A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 829, doi. 10.1038/sj.ejhg.5201186
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- Publication type:
- Article
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 797, doi. 10.1038/sj.ejhg.5201203
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- Publication type:
- Article
Detection of the founder effect in Finnish CADASIL families.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 813, doi. 10.1038/sj.ejhg.5201221
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- Publication type:
- Article
Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 855, doi. 10.1038/sj.ejhg.5201225
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- Publication type:
- Article
1024C>T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family.
- Published in:
- 2004
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- Publication type:
- Letter
QTLs for height: results of a full genome scan in Dutch sibling pairs.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 820, doi. 10.1038/sj.ejhg.5201229
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- Publication type:
- Article
RNAi of COL1A1 in mesenchymal progenitor cells.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 864, doi. 10.1038/sj.ejhg.5201230
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- Publication type:
- Article
Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 805, doi. 10.1038/sj.ejhg.5201233
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- Publication type:
- Article
Paraoxonase 1 polymorphisms and survival.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 843, doi. 10.1038/sj.ejhg.5201235
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- Publication type:
- Article
Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 867, doi. 10.1038/sj.ejhg.5201245
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- Publication type:
- Article
Congenital deficiency of alpha feto-protein.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 871, doi. 10.1038/sj.ejhg.5201246
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- Publication type:
- Article
Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 835, doi. 10.1038/sj.ejhg.5201248
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- Publication type:
- Article
Breast cancer: role of polymorphisms in biotransformation enzymes.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 848, doi. 10.1038/sj.ejhg.5201249
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- Publication type:
- Article
Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 790, doi. 10.1038/sj.ejhg.5201252
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- Publication type:
- Article