الماجستير

دكتوراه

بكالوريوس

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

نوع النشر:مجلة علمية

الناشر:Journal of Assisted Reproduction and Genetics

01/12/2013

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

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

نوع النشر:مجلة علمية

الناشر:Molecular Genetics and Metabolism

01/11/2013

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

نوع النشر:مجلة علمية

الناشر:SCLA

23/06/2013

Mahayri Z. , Monem F.

Screening GJB2 Gene Mutations in Syrians with Sensorinural Hearing Loss

نوع النشر:مجلة علمية

الناشر:Middle East Journal of Human Genetics

01/07/2012

Mahayri Z. , Monem F.

A Review of 1125 cases referred for cytogenetic analysis in Syria

نوع النشر:مجلة علمية

الناشر:Middle East Journal of Human Genetics

01/01/2012

Mahayri Z. , Monem F.

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

أخرى

الدولة:سوريا

01/12/2013

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

أخرى

الدولة:أخرى

01/11/2013

First international Conference of Human Genetics & Genome

مشاركة في مؤتمر/ندوة

الدولة:مصر

01/11/2010

International Training Course on Microarray Technology for Gene Discovery and Expression

حضور دورة

الدولة:باكستان

15/09/2009

Medicare

مشاركة في مؤتمر/ندوة

الدولة:سوريا

01/06/2008