Works matching IS 11108630 AND DT 2016 AND VI 17 AND IP 2
Results: 15
Fraser syndrome: Phenotypic variability and unusual findings in four Egyptian families.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 233, doi. 10.1016/j.ejmhg.2015.10.004
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- Publication type:
- Article
Partial association of restriction polymorphism of the ligand binding domain of human androgen receptor in prostate cancer.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 223, doi. 10.1016/j.ejmhg.2015.09.004
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- Article
CORRIGENDUM.
- Published in:
- 2016
- Publication type:
- Correction Notice
Griscelli syndrome type 2 - A case report and clinical approach to silver blonde hair.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 229, doi. 10.1016/j.ejmhg.2015.08.008
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- Publication type:
- Article
Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 217, doi. 10.1016/j.ejmhg.2015.09.003
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- Publication type:
- Article
Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 209, doi. 10.1016/j.ejmhg.2015.09.002
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- Publication type:
- Article
Inducible protective processes in animal systems XIV: Cytogenetic adaptive response induced by EMS or MMS in bone marrow cells of diabetic mouse.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 201, doi. 10.1016/j.ejmhg.2015.12.007
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- Publication type:
- Article
Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 197, doi. 10.1016/j.ejmhg.2015.12.004
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- Publication type:
- Article
The association between (8390G>A) single nucleotide polymorphism in APOE gene with Alzheimer's and Parkinson disease.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 185, doi. 10.1016/j.ejmhg.2015.11.003
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- Publication type:
- Article
Sirtuin 1 gene rs2273773 C >T single nucleotide polymorphism and protein oxidation markers in asthmatic patients.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 191, doi. 10.1016/j.ejmhg.2015.12.002
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- Publication type:
- Article
Inducible protective processes in animal systems XV: Hyperthermia enhances the Ethyl methanesulfonate induced adaptive response in meiotic cells of grasshopper Poecilocerus pictus.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 173, doi. 10.1016/j.ejmhg.2015.11.002
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- Publication type:
- Article
Molecular characterization of X chromosome fragility in idiopathic mental retardation.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 165, doi. 10.1016/j.ejmhg.2015.11.001
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- Publication type:
- Article
Cytokine gene polymorphisms and their association with cervical cancer: A North Indian study.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 155, doi. 10.1016/j.ejmhg.2015.10.005
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- Publication type:
- Article
Natural killer cells enhance the immune surveillance of cancer.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 149, doi. 10.1016/j.ejmhg.2015.08.006
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- Publication type:
- Article
Role of MTHFR A1298C gene polymorphism in the etiology of prostate cancer: A systematic review and updated meta-analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 141, doi. 10.1016/j.ejmhg.2015.06.005
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- Publication type:
- Article