Patenting and licensing in genetic testing.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 405, doi. 10.1038/sj.ejhg.5201929
- By:
- Publication type:
- Article
Works matching IS 10184813 AND DT 2008 AND VI 16 AND IP 4
Results: 16
1
2
The exon 1–8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 480, doi. 10.1038/sj.ejhg.5201948
- By:
- Publication type:
- Article
3
8q24 and prostate cancer: association with advanced disease and meta-analysis.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 496, doi. 10.1038/sj.ejhg.5201959
- By:
- Publication type:
- Article
4
‘It is not in my world’: an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 435, doi. 10.1038/sj.ejhg.5201965
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- Publication type:
- Article
5
Recreational genomics? Dreams and fears on genetic susceptibility screening.
- Published in:
- 2008
- By:
- Publication type:
- Editorial
6
How molecular genetics and other disciplines pushed forward understanding our past: Before the Dawn (Recovering the Lost History of Our Ancestors).
- Published in:
- 2008
- By:
- Publication type:
- Book Review
7
Empirical assessment of the validity of the ‘fundamental theorem of the HapMap’ in the light of ‘cryptic’ tagging of multiple susceptibility loci.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 525, doi. 10.1038/sj.ejhg.5201984
- By:
- Publication type:
- Article
8
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 471, doi. 10.1038/sj.ejhg.5201986
- By:
- Publication type:
- Article
9
Singleton SNPs in the human genome and implications for genome-wide association studies.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 506, doi. 10.1038/sj.ejhg.5201987
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- Publication type:
- Article
10
What is ideal genetic counselling? A survey of current international guidelines.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 445, doi. 10.1038/sj.ejhg.5201983
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- Publication type:
- Article
11
Imputing missing genotypic data of single-nucleotide polymorphisms using neural networks.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 487, doi. 10.1038/sj.ejhg.5201988
- By:
- Publication type:
- Article
12
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 516, doi. 10.1038/sj.ejhg.5201992
- By:
- Publication type:
- Article
13
XLMR genes: update 2007.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 422, doi. 10.1038/sj.ejhg.5201994
- By:
- Publication type:
- Article
14
Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 453, doi. 10.1038/sj.ejhg.5201993
- By:
- Publication type:
- Article
15
Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 462, doi. 10.1038/sj.ejhg.5201995
- By:
- Publication type:
- Article
16
Smith–Magenis syndrome.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 412, doi. 10.1038/sj.ejhg.5202009
- By:
- Publication type:
- Article