Found: 15
Select item for more details and to access through your institution.
Non-invasive prenatal screening for chromosomal abnormalities using circulating cell-free fetal DNA in maternal plasma: Current applications, limitations and prospects.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 1, doi. 10.1016/j.ejmhg.2016.07.004
- By:
- Publication type:
- Article
Strength training versus chest physical therapy on pulmonary functions in children with Down syndrome.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 35, doi. 10.1016/j.ejmhg.2016.02.008
- By:
- Publication type:
- Article
Parathyroid hormone in pediatric patients with β-thalassemia major and its relation to βone mineral density; a case control study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 75, doi. 10.1016/j.ejmhg.2016.03.004
- By:
- Publication type:
- Article
Study of obesity associated proopiomelanocortin gene polymorphism: Relation to metabolic profile and eating habits in a sample of obese Egyptian children and adolescents.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 67, doi. 10.1016/j.ejmhg.2016.02.009
- By:
- Publication type:
- Article
Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 87, doi. 10.1016/j.ejmhg.2015.12.001
- By:
- Publication type:
- Article
Clinical profile of cyanotic congenital heart disease in neonatal intensive care unit at Sohag University Hospital, Upper Egypt.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 47, doi. 10.1016/j.ejmhg.2016.01.003
- By:
- Publication type:
- Article
Risk factors for congenital anomalies in high risk pregnant women: A large study from South India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 79, doi. 10.1016/j.ejmhg.2016.04.001
- By:
- Publication type:
- Article
The β fiβrinogen gene G-455A polymorphism in Asian suβjects with coronary heart disease: A meta analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 19, doi. 10.1016/j.ejmhg.2016.06.002
- By:
- Publication type:
- Article
Mitochondrial control region and GSTP1 polymorphism associated with familial urinary bladder cancer in Karbi-Anglong tribe of Assam, Northeast India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 99, doi. 10.1016/j.ejmhg.2016.02.002
- By:
- Publication type:
- Article
Role of TLR4 gene polymorphisms in the colorectal cancer risk modulation in ethnic Kashmiri population - A case-control study.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
MTRR gene variants may predispose to the risk of Congenital Heart Disease in Down syndrome patients of Indian origin.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 61, doi. 10.1016/j.ejmhg.2016.02.006
- By:
- Publication type:
- Article
Null association of maternal MTHFR A1298C polymorphism with Down syndrome pregnancy: An updated meta-analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 9, doi. 10.1016/j.ejmhg.2016.04.003
- By:
- Publication type:
- Article
C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot's spots and agenesis of the corpus callosum in an Egyptian child.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Association between interleukin-4 (IL-4), gene polymorphisms (C-589T, T+2979G, and C-33T) and migraine susceptibility in Iranian population: A case-control study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 29, doi. 10.1016/j.ejmhg.2016.05.001
- By:
- Publication type:
- Article
Genotypes of GSTM1 and GSTT1: Useful determinants for clinical outcome of bladder cancer in Pakistani population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 41, doi. 10.1016/j.ejmhg.2016.03.001
- By:
- Publication type:
- Article