Allergic rhinitis and genetic components: focus on Toll-like receptors (TLRs) gene polymorphism.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 109, doi. 10.2147/TACG.S8380
- By:
- Publication type:
- Article
Works matching IS 1178704X AND DT 2010 AND VI 3
Results: 15
1
2
Psychogenetics of post-traumatic stress disorder: a short review.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 103, doi. 10.2147/TACG.S13926
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- Publication type:
- Article
3
Diagnostic criteria, specific mutations, and genetic predisposition in gastrointestinal stromal tumors.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 85, doi. 10.2147/TACG.S7191
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- Publication type:
- Article
4
Disorders caused by chromosome abnormalities.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 159, doi. 10.2147/TACG.S8884
- By:
- Publication type:
- Article
5
Genetic screening for homozygous and heterozygous familial hypercholesterolemia.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 147, doi. 10.2147/TACG.S13490
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- Publication type:
- Article
6
Recent developments in the treatment of acute abdominal and facial attacks of hereditary angioedema: focus on human C1 esterase inhibitor.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 133, doi. 10.2147/TACG.S9275
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- Publication type:
- Article
7
Management of the asymptomatic BRCA mutation carrier.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 121, doi. 10.2147/TACG.S8882
- By:
- Publication type:
- Article
8
The genetic basis of familial hypercholesterolemia: inheritance, linkage, and mutations.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 53
- By:
- Publication type:
- Article
9
Genetic contribution and associated pathophysiology in end-stage renal disease.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 65
- By:
- Publication type:
- Article
10
Genetic and molecular mechanisms in multiple myeloma: a route to better understand disease pathogenesis and heterogeneity.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 41
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- Publication type:
- Article
11
Congenital malformations in Ecuadorian children: urgent need to create a National Registry of Birth Defects.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 29
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- Publication type:
- Article
12
Amniotic band syndrome and/or limb body wall complex: split or lump.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 7
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- Publication type:
- Article
13
Gene polymorphisms in association with self-reported stroke in US adults.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 23
- By:
- Publication type:
- Article
14
Pilot study of an association between a common variant in the non-muscle myosin heavy chain 9 (MYH9) gene and type 2 diabetic nephropathy in a Taiwanese population.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 17
- By:
- Publication type:
- Article
15
Inheritance of craniofacial features in Colombian families with class III malocclusion.
- Published in:
- Application of Clinical Genetics, 2010, v. 3, p. 1
- By:
- Publication type:
- Article