Works matching IS 10184813 AND DT 2010 AND VI 18 AND IP 3
Results: 21
Triple X syndrome: a review of the literature.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 265, doi. 10.1038/ejhg.2009.109
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- Article
Methionine synthase A2756G polymorphism and cancer risk: a meta-analysis.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 370, doi. 10.1038/ejhg.2009.131
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- Article
Research and applied medical genetics: filling the gap.
- Published in:
- 2010
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- Publication type:
- Book Review
‘Me, Myself, and Why. Understanding your own genome and evolutionary history’.
- Published in:
- 2010
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- Publication type:
- Book Review
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 296, doi. 10.1038/ejhg.2009.155
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- Article
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 342, doi. 10.1038/ejhg.2009.157
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- Article
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 285, doi. 10.1038/ejhg.2009.159
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- Article
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 291, doi. 10.1038/ejhg.2009.163
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- Article
The emergence of Y-chromosome haplogroup J1e among Arabic-speaking populations.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 348, doi. 10.1038/ejhg.2009.166
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- Publication type:
- Article
A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 379, doi. 10.1038/ejhg.2009.167
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- Article
Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 354, doi. 10.1038/ejhg.2009.168
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- Article
Functional consequences of mitochondrial tRNA<sup>Trp</sup> and tRNA<sup>Arg</sup> mutations causing combined OXPHOS defects.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 324, doi. 10.1038/ejhg.2009.169
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- Article
Understanding sickle cell carrier status identified through newborn screening: a qualitative study.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 303, doi. 10.1038/ejhg.2009.173
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- Article
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 278, doi. 10.1038/ejhg.2009.174
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- Publication type:
- Article
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 330, doi. 10.1038/ejhg.2009.175
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- Publication type:
- Article
Genetic variants in human CLOCK associate with total energy intake and cytokine sleep factors in overweight subjects (GOLDN population).
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 364, doi. 10.1038/ejhg.2009.176
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- Publication type:
- Article
Large-scale parent–child comparison confirms a strong paternal influence on telomere length.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 385, doi. 10.1038/ejhg.2009.178
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- Publication type:
- Article
Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 336, doi. 10.1038/ejhg.2009.179
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- Publication type:
- Article
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 309, doi. 10.1038/ejhg.2009.180
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- Publication type:
- Article
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 317, doi. 10.1038/ejhg.2009.181
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- Publication type:
- Article
Non-invasive prenatal testing: ethical issues explored.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 272, doi. 10.1038/ejhg.2009.203
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- Article