Works matching IS 11108630 AND DT 2017 AND VI 18 AND IP 1

Results: 15

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:

Costa, Cláudia Amorim

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:

Hussein, Zeinab Ahmed

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:

El-Nashar, Mostafa;
Mortagy, Ahmed Kamel;
El-Beblawy, Nagham M. S.;
El-Gohary, Eman;
Kamel, Irene Mokhtar;
Rashad, Mona;
Mouharam, Wessam A.

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:

El-Baz Mohamed, Farida;
Hamza, Rasha T.;
Amr, Nermine H.;
Youssef, Azza M.;
Kamal, Tarek M.;
Mahmoud, Rana A.

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:

Abou-Taleb, Ashraf;
Abdelhamid, Marwa A.;
Bahkeet, Mohamed A. M.

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:

Sunitha, Tella;
Prasoona, Kattekola Rebekah;
Kumari, Tiruvatturu Muni;
Srinadh, Buragadda;
Madireddy Laxmi Naga Deepika;
Aruna, Ramaiah;
Jyothy, Akka

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:

Rai, Vandana;
Yadav, Upendra;
Kumar, Pradeep

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:

Malik, Saima Shakil;
Nawaz, Gul;
Masood, Nosheen

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:

Shawky, Rabah M.;
Gamal, Radwa;
Mostafa, Nayera

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:

Fajar, Jonny Karunia

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:

Nissar, Saniya;
Sameer, Aga Syed;
Rasool, Roohi;
Qadri, Qurteeba;
Chowdri, Nissar A.;
Rashid, Fouzia

Publication type:

Case Study

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:

Ghatak, Souvik;
Yadav, Ravi Prakash;
Rathore, Hanumath Singh;
Thou, Keheibamding;
Jakha, Felix;
Sumi, K. Toska;
Sanga, Zothan;
Kumar, Nachimuthu Senthil

Publication type:

Article

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:

Asim, Ambreen;
Agarwal, Sarita;
Panigrahi, Inusha

Publication type:

Article

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:

Ramroodi, Nourollah;
Javan, Mohammad Reza;
Sanadgol, Nima;
Jahantigh, Mehdi;
Khodakheir, Tooba Nakhzari;
Ranjbar, Nasrin

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:

Shawky, Rabah M.;
Gamal, Radwa

Publication type:

Case Study