Works matching IS 10184813 AND DT 2008 AND VI 16 AND IP 9
Results: 21
Patenting and licensing in genetic testing: Recommendations of the European Society of Human Genetics.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1159, doi. 10.1038/ejhg.2008.123
- Publication type:
- Article
Quantifying the increase in average human heterozygosity due to urbanisation.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1097, doi. 10.1038/ejhg.2008.48
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- Publication type:
- Article
Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–13.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1103, doi. 10.1038/ejhg.2008.50
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- Publication type:
- Article
Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1062, doi. 10.1038/ejhg.2008.52
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- Publication type:
- Article
Composite measure of linkage disequilibrium for testing interaction between unlinked loci.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
Catechol O-methyl transferase and dopamine D2 receptor gene polymorphisms: evidence of positive heterosis and gene–gene interaction on working memory functioning.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1075, doi. 10.1038/ejhg.2008.57
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- Publication type:
- Article
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1050, doi. 10.1038/ejhg.2008.58
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- Publication type:
- Article
Cox proportional hazards models have more statistical power than logistic regression models in cross-sectional genetic association studies.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1111, doi. 10.1038/ejhg.2008.59
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- Publication type:
- Article
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1055, doi. 10.1038/ejhg.2008.60
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- Publication type:
- Article
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1117, doi. 10.1038/ejhg.2008.62
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- Publication type:
- Article
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1126, doi. 10.1038/ejhg.2008.64
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- Publication type:
- Article
MCT8 mutation analysis and identification of the first female with Allan–Herndon–Dudley syndrome due to loss of MCT8 expression.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1029, doi. 10.1038/ejhg.2008.66
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- Publication type:
- Article
Interleukin 18 receptor 1 gene polymorphisms are associated with asthma.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1083, doi. 10.1038/ejhg.2008.67
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- Publication type:
- Article
Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1038, doi. 10.1038/ejhg.2008.68
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- Publication type:
- Article
Reconstructing the phylogeny of African mitochondrial DNA lineages in Slavs.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1091, doi. 10.1038/ejhg.2008.70
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- Publication type:
- Article
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1135, doi. 10.1038/ejhg.2008.72
- By:
- Publication type:
- Article
Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1070, doi. 10.1038/ejhg.2008.73
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- Publication type:
- Article
Evaluation of HapMap data in six populations of European descent.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1142, doi. 10.1038/ejhg.2008.77
- By:
- Publication type:
- Article
Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1151, doi. 10.1038/ejhg.2008.86
- By:
- Publication type:
- Article
An Xp11.23 deletion containing PORCN may also cause angioma serpiginosum, a cosmetic skin disease associated with extreme skewing of X-inactivation.
- Published in:
- 2008
- By:
- Publication type:
- Letter
HuGE Watch: tracking trends and patterns of published studies of genetic association and human genome epidemiology in near-real time.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1155, doi. 10.1038/ejhg.2008.95
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- Publication type:
- Article