Works matching IS 11108630 AND DT 2013 AND VI 14 AND IP 2
Results: 15
Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 177, doi. 10.1016/j.ejmhg.2012.10.008
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- Publication type:
- Article
Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 171, doi. 10.1016/j.ejmhg.2013.01.001
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- Article
Analysis of aromatase (CYP19) gene in Iranian women with endometriosis.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 165, doi. 10.1016/j.ejmhg.2012.10.002
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- Article
Consanguinity and its relevance to clinical genetics.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 157, doi. 10.1016/j.ejmhg.2013.01.002
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- Article
Novel mutation predicted to disrupt SGOL1 protein function.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 149, doi. 10.1016/j.ejmhg.2012.09.001
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- Article
Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 143, doi. 10.1016/j.ejmhg.2013.01.005
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- Publication type:
- Article
Computational evaluation of small molecule inhibitors of RGS4 to regulate the dopaminergic control of striatal LTD.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 135, doi. 10.1016/j.ejmhg.2012.10.007
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- Article
Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 123, doi. 10.1016/j.ejmhg.2012.08.001
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- Publication type:
- Article
Basic concepts of medical genetics, pathogenetics, part 3.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 209, doi. 10.1016/j.ejmhg.2012.12.001
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- Article
Gene frequency of sickle cell trait among Muslim populations in a Malarial belt of India, i.e., Manipur.
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- 2013
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- Publication type:
- Letter
Letter to the editor: Controversial report on sickle cell trait in Manipur, India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 205, doi. 10.1016/j.ejmhg.2012.11.005
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- Article
Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 201, doi. 10.1016/j.ejmhg.2012.10.005
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- Publication type:
- Article
Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 195, doi. 10.1016/j.ejmhg.2012.11.003
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- Publication type:
- Article
Evaluation of micronucleus frequency by acridine orange fluorescent staining in bucccal epithelial cells of oral submucosus fibrosis (OSMF) patients.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 189, doi. 10.1016/j.ejmhg.2012.11.004
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- Article
Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 2, p. 183, doi. 10.1016/j.ejmhg.2012.11.001
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- Publication type:
- Article