Works matching IS 11108630 AND DT 2016 AND VI 17 AND IP 1
Results: 18
Distribution of ABO blood groups and rhesus factor in a Large Scale Study of different cities and ethnicities in Khuzestan province, Iran.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 105, doi. 10.1016/j.ejmhg.2015.07.004
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- Publication type:
- Article
Do the MTHFR gene polymorphism and Down syndrome pregnancy association stands true? A case-control study of Indian population and meta-analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 87, doi. 10.1016/j.ejmhg.2015.08.003
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- Publication type:
- Article
Circulating cell free DNA as a predictor of systemic lupus erythematosus severity and monitoring of therapy.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 79, doi. 10.1016/j.ejmhg.2015.07.001
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- Publication type:
- Article
α-4 subunit of nicotinic acetylcholine receptor polymorphisms exhibit no association with smoking behavior among Malay Males in Kelantan, Malaysia.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 71, doi. 10.1016/j.ejmhg.2015.08.002
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- Publication type:
- Article
Apolipoprotein E gene polymorphism in Egyptian acute coronary syndrome patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 99, doi. 10.1016/j.ejmhg.2015.08.001
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- Publication type:
- Article
Cytogenetic diagnosis of Roberts SC phocomelia syndrome: First report from Kashmir.
- Published in:
- 2016
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- Publication type:
- Case Study
Screening of a clinically and biochemically diagnosed SOD patient using exome sequencing: A case report with a mutations/variations analysis approach.
- Published in:
- 2016
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- Publication type:
- Case Study
Opitz C syndrome: Trigonocephaly, mental retardation and craniofacial dysmorphism.
- Published in:
- 2016
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- Publication type:
- Case Study
Baraitser-Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum.
- Published in:
- 2016
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- Publication type:
- Case Study
Exploring the link between VDR rs2228570 and uterine leiomyoma in Iranian women.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 115, doi. 10.1016/j.ejmhg.2015.08.007
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- Publication type:
- Article
Susceptibility to methamphetamine dependence associated with high transcriptional activity alleles of VNTR polymorphism in the promoter region of monoamine oxidase A (MAOA).
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 111, doi. 10.1016/j.ejmhg.2015.08.004
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- Publication type:
- Article
Magnesium supplementation in children with attention deficit hyperactivity disorder.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 63, doi. 10.1016/j.ejmhg.2015.05.008
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- Publication type:
- Article
Chromosomal abnormalities and autism.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 57, doi. 10.1016/j.ejmhg.2015.05.002
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- Publication type:
- Article
Pilot study for early prognosis of Azoospermia in relation to Y-STR Profiling.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 47, doi. 10.1016/j.ejmhg.2015.06.004
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- Publication type:
- Article
Cyclooxygenase 1 (COX1) expression in Type 2 diabetes mellitus: A preliminary study from north India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 41, doi. 10.1016/j.ejmhg.2015.07.003
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- Publication type:
- Article
Association of −308G/A TNF-α gene polymorphism and spontaneous preterm birth in Acehnese ethnic group, Indonesia: This polymorphism is not associated with preterm birth.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 33, doi. 10.1016/j.ejmhg.2015.05.001
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- Publication type:
- Article
Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 25, doi. 10.1016/j.ejmhg.2015.07.005
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- Publication type:
- Article
Pathogenetics. An introductory review.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 1, doi. 10.1016/j.ejmhg.2015.07.002
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- Publication type:
- Article