Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major 70A→G mutation of the untranslated RMRP.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 439
- By:
- Publication type:
- Article
Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 7
Results: 7
1
2
Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 433, doi. 10.1038/sj.ejhg.5200830
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- Publication type:
- Article
3
Connexin 26 mutations in cases of sensorineural deafness in eastern Austria.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 427, doi. 10.1038/sj.ejhg.5200826
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- Publication type:
- Article
4
WFS1 mutations in Spanish patients with diabetes mellitus and deafness.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 421
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- Publication type:
- Article
5
The 3'-untranslated region of the dystrophin gene--conservation and consequences of loss.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 412, doi. 10.1038/sj.ejhg.5200822
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- Publication type:
- Article
6
Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 406, doi. 10.1038/sj.ejhg.5200815
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- Publication type:
- Article
7
Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 7, p. 399, doi. 10.1038/sj.ejhg.5200820
- By:
- Publication type:
- Article