Found: 7
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A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness.
- Published in:
- Audiology & Neurotology, 2004, v. 9, n. 1, p. 47, doi. 10.1159/000074186
- By:
- Publication type:
- Article
The rs2516839 variation of USF1 gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 1, p. 34, doi. 10.1111/ahg.12282
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- Publication type:
- Article
A novel protein involved in heart development in Ambystoma mexicanum is localized in endoplasmic reticulum.
- Published in:
- Journal of Biomedical Science, 2008, v. 15, n. 6, p. 789, doi. 10.1007/s11373-008-9262-y
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- Publication type:
- Article
Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 1, p. 66, doi. 10.1034/j.1399-0004.2002.610113.x
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- Publication type:
- Article
CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population.
- Published in:
- European Journal of Neurology, 2012, v. 19, n. 5, p. 769, doi. 10.1111/j.1468-1331.2011.03639.x
- By:
- Publication type:
- Article
LRRK2 mutations are uncommon in Turkey.
- Published in:
- 2011
- By:
- Publication type:
- Letter