Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 11
Results: 15
Genetic analysis of the GRM1 gene in human melanoma susceptibility.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1176, doi. 10.1038/sj.ejhg.5201887
- By:
- Publication type:
- Article
A new mutation in TP63 is associated with age-related pathology.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1115, doi. 10.1038/sj.ejhg.5201888
- By:
- Publication type:
- Article
The efficiency of nonsense-mediated mRNA decay is an inherent character and varies among different cells.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1156, doi. 10.1038/sj.ejhg.5201889
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- Publication type:
- Article
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1145, doi. 10.1038/sj.ejhg.5201891
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- Publication type:
- Article
Co-introgression of Y-chromosome haplogroups and the sickle cell gene across Africa's Sahel.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1183, doi. 10.1038/sj.ejhg.5201892
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- Publication type:
- Article
Risk estimation for familial breast cancer: improving the system of counselling.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1139, doi. 10.1038/sj.ejhg.5201895
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- Publication type:
- Article
Guidelines for molecular karyotyping in constitutional genetic diagnosis.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1105, doi. 10.1038/sj.ejhg.5201896
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- Publication type:
- Article
A functional mutation in the LDLR promoter (−139C>G) in a patient with familial hypercholesterolemia.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1186, doi. 10.1038/sj.ejhg.5201897
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- Publication type:
- Article
Consent and confidentiality: Consent and Confidentiality in Genetic Practice.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf–Hirschhorn syndrome.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1132, doi. 10.1038/sj.ejhg.5201899
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- Publication type:
- Article
Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1121, doi. 10.1038/sj.ejhg.5201900
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- Publication type:
- Article
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1163, doi. 10.1038/sj.ejhg.5201901
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- Publication type:
- Article
Two-stage association tests for genome-wide association studies based on family data with arbitrary family structure.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1169, doi. 10.1038/sj.ejhg.5201902
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- Publication type:
- Article
Deletions Revealing Recessive Genes: Deletions that reveal recessive genes.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1103, doi. 10.1038/sj.ejhg.5201919
- By:
- Publication type:
- Article
In memoriam: Dr Marina Seabright.
- Published in:
- 2007
- By:
- Publication type:
- Obituary