Works matching IS 03406717 AND DT 2008 AND VI 123 AND IP 2
Results: 11
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 177, doi. 10.1007/s00439-007-0460-x
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- Publication type:
- Article
Michael H. Crawford (ed): Anthropological genetics.
- Published in:
- 2008
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- Publication type:
- Book Review
Genetic variation in CYP17 and endometrial cancer risk.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 155, doi. 10.1007/s00439-007-0454-8
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- Article
The MTHFR gene polymorphism is associated with lean body mass but not fat body mass.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 189, doi. 10.1007/s00439-007-0463-7
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- Publication type:
- Article
The Environmental Polymorphisms Registry: a DNA resource to study genetic susceptibility loci.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 207, doi. 10.1007/s00439-007-0457-5
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- Publication type:
- Article
Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2–q22.1 in an inbred Pakistani family.
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- Human Genetics, 2008, v. 123, n. 2, p. 197, doi. 10.1007/s00439-007-0458-4
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- Publication type:
- Article
Identifying susceptibility loci for nicotine dependence: 2008 update based on recent genome-wide linkage analyses.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 119, doi. 10.1007/s00439-008-0473-0
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- Publication type:
- Article
Significant association of DRD1 with nicotine dependence.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 133, doi. 10.1007/s00439-007-0453-9
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- Publication type:
- Article
Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophy.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 141, doi. 10.1007/s00439-007-0455-7
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- Publication type:
- Article
The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 163, doi. 10.1007/s00439-007-0456-6
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- Publication type:
- Article
Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study.
- Published in:
- Human Genetics, 2008, v. 123, n. 2, p. 215, doi. 10.1007/s00439-008-0465-0
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- Publication type:
- Article