الماجستير

دكتوراه

بكالوريوس

High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia

Publication Type:Journal

Publisher:Journal of Assisted Reproduction and Genetics

12/1/2013

Halabi M., Kenj M., Monem F., Mahayri Z., Abou AlChamat G., Madania A.

“Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa“

Publication Type:Journal

Publisher:Molecular Genetics and Metabolism

11/1/2013

1. Dimpopoulou A, Fischer B, Gardeitchik T, Schröter P, Kayserili H, Schlack C, Li Y, Brum J, Barisic I, Castori M, Spaich C, Fletcher E, Mahayri Z, Bhat M, Girisha K, Lachlan K, Parker M, Phadke S, Gupta N, Simandlova M, Kabra M, David A, Nijtmans L, Chitayat D, Tuysuz B, Brancati F, Mundlos S, Maldergem L, Morava E, Wollnik B.

Study of GJB2 Gene Mutations in Syrians with Hearing Loss: High frequency of consanguinity and limited concern of genetic tests

Publication Type:Journal

Publisher:SCLA

6/23/2013

Mahayri Z. , Monem F.

Screening GJB2 Gene Mutations in Syrians with Sensorinural Hearing Loss

Publication Type:Journal

Publisher:Middle East Journal of Human Genetics

7/1/2012

Mahayri Z. , Monem F.

A Review of 1125 cases referred for cytogenetic analysis in Syria

Publication Type:Journal

Publisher:Middle East Journal of Human Genetics

1/1/2012

Mahayri Z. , Monem F.

High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia

Others

Country:سوريا

12/1/2013

Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa

Others

Country:أخرى

11/1/2013

First international Conference of Human Genetics & Genome

Conference Participation

Country:مصر

11/1/2010

International Training Course on Microarray Technology for Gene Discovery and Expression

Course Participation

Country:باكستان

9/15/2009

Medicare

Conference Participation

Country:سوريا

6/1/2008