Works matching IS 11108630 AND DT 2016 AND VI 17 AND IP 1

Results: 18

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

By:

Saify, Khyber;
Saadat, Mostafa

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

By:

Mahmoud, Aida A.;
Yousef, Laila M.;
Elhamed Zaki, Nayl Abd

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

By:

Muthuswamy, Srinivasan;
Agarwal, Sarita

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

By:

Ruzilawati, A. B.;
Rozak, N. I. Abd;
Norsuhaily, A. B.;
Imran, A.

Publication type:

Article

Cytogenetic diagnosis of Roberts SC phocomelia syndrome: First report from Kashmir.

Published in:

2016

By:

Malla, Tahir M.;
Pandith, Arshad A.;
Dar, Fayaz A.;
Zargar, Mahrukh H.

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

By:

Aghanoori, Mohamad-Reza;
Shahriary, Ghazaleh Mohammadzadeh;
Safarpour, Mahdi;
Ebrahimi, Ahmad

Publication type:

Case Study

Opitz C syndrome: Trigonocephaly, mental retardation and craniofacial dysmorphism.

Published in:

2016

By:

Fierro, J. A. Avina;
Avina, D. A. Hernandez

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

By:

Shawky, Rabah M.;
Gamal, Radwa;
Mohammad, Shaimaa Abdelsattar

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

By:

Shahbazi, Shirin

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

By:

Baza, Farida El;
AlShahawi, Heba Ahmed;
Zahra, Sally;
AbdelHakim, Rana Ahmed

Publication type:

Article

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

By:

maatoghi, J. Torabizade;
Paridar, M.;
Shoushtari, M. Mahmodian;
Kiani, B.;
Nori, B.;
Shahjahani, M.;
Khosravi, A.;
Kelarijani, N. Amani;
Ghalesardi, O. Kiani;
Far, M. A. Jalali

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

By:

El-Baz, Farida;
Zaghloul, Mohamed Saad;
Sobky, Ezzat El;
Elhossiny, Reham M.;
Salah, Heba;
Abdelaziz, Neveen Ezy

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

By:

Refaat, Ahmed M.

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

By:

Hendy, Olfat M.;
Motalib, Tawfik Abdel;
El Shafie, Mona A.;
Khalaf, Fatma A.;
Kotb, Sobhy E.;
Khalil, Aziza;
Ali, Salwa R.

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

By:

Andalas, Mohd;
Hakimi, Mohammad;
Nurdiati, Detty Siti;
Astuti, Indwiani;
Imran, Imran;
Harapan, Harapan

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

By:

Malla, Tahir M.;
Dar, Fayaz A.;
Pandith, Arshad A.;
Zargar, Mahrukh H.

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

By:

Zaghloul Salem, Mohammad Saad

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

By:

Verma, Sushma;
Chandra, Honey;
Banerjee, Monisha

Publication type:

Article