Works matching IS 10184813 AND DT 2009 AND VI 17 AND IP 7
Results: 17
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 911, doi. 10.1038/ejhg.2008.213
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- Publication type:
- Article
Genomics and breast cancer: the different levels of inherited susceptibility.
- Published in:
- 2009
- By:
- Publication type:
- Opinion
Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 857, doi. 10.1038/ejhg.2008.246
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- Publication type:
- Article
An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 890, doi. 10.1038/ejhg.2008.253
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- Publication type:
- Article
Personal genomics services: whose genomes?
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 883, doi. 10.1038/ejhg.2008.254
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- Publication type:
- Article
Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 958, doi. 10.1038/ejhg.2008.260
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- Publication type:
- Article
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 904, doi. 10.1038/ejhg.2008.261
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- Publication type:
- Article
The complex interaction between APOE promoter and AD: an Italian case–control study.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 938, doi. 10.1038/ejhg.2008.263
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- Publication type:
- Article
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 946, doi. 10.1038/ejhg.2008.264
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- Publication type:
- Article
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 897, doi. 10.1038/ejhg.2008.265
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- Publication type:
- Article
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 967, doi. 10.1038/ejhg.2008.266
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- Publication type:
- Article
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 928, doi. 10.1038/ejhg.2008.270
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- Publication type:
- Article
Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 919, doi. 10.1038/ejhg.2008.271
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- Publication type:
- Article
Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 872, doi. 10.1038/ejhg.2009.33
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- Publication type:
- Article
Hereditary haemorrhagic telangiectasia: a clinical and scientific review.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 860, doi. 10.1038/ejhg.2009.35
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- Publication type:
- Article
Reply to Happle.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Angioma serpiginosum is not caused by PORCN mutations.
- Published in:
- 2009
- By:
- Publication type:
- Letter