Various Uses for DNA Variations.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 153, doi. 10.1038/sj.ejhg.5200774
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- Publication type:
- Article
Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 2
Results: 13
1
2
BRCA mutations in Italian breast/ovarian cancer families.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 150, doi. 10.1038/sj.ejhg.5200755
- Publication type:
- Article
3
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever.
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- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 145, doi. 10.1038/sj.ejhg.5200776
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- Publication type:
- Article
4
Leigh disease associated with a novel mitochondrial DNA ND5 mutation.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 141, doi. 10.1038/sj.ejhg.5200773
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- Publication type:
- Article
5
Do reduced levels of steroid 21-hydroxylase confer a survival advantage in fetuses affected by sex chromosome aberrations?
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- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 137, doi. 10.1038/sj.ejhg.5200778
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- Publication type:
- Article
6
An evaluation of the variance components approach: type 1 error, power and size of the estimated effect.
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- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 133, doi. 10.1038/sj.ejhg.5200772
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- Publication type:
- Article
7
Optimal selection strategies for QTL mapping using pooled DNA samples.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 125, doi. 10.1038/sj.ejhg.5200771
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- Publication type:
- Article
8
A centenarian-only approach for assessing gene-gene interaction in human longevity.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 119, doi. 10.1038/sj.ejhg.5200770
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- Publication type:
- Article
9
Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos.
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- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 113, doi. 10.1038/sj.ejhg.5200767
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- Publication type:
- Article
10
A human interstitial telomere associates in vivo with specific TRF2 and TIN2 proteins.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 107, doi. 10.1038/sj.ejhg.5200775
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- Publication type:
- Article
11
Determination of the relative contribution of three genes--the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene--to the etiology of idiopathic chronic...
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 100
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- Publication type:
- Article
12
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 95, doi. 10.1038/sj.ejhg.5200769
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- Publication type:
- Article
13
Merosin-deficient congenital muscular dystrophy autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin).
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 2, p. 91, doi. 10.1038/sj.ejhg.5200743
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- Publication type:
- Article