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The single nucleotide polymorphism rs2305957 G/A is not associated with recurrent pregnancy loss

Sharif, Fadel A.; Ashour, Mohammed J. (2017)

Background: This study was conducted in order to investigate the association between the single nucleotide polymorphism (SNP) rs2305957 G/A and recurrent pregnancy loss (RPL) in a group of Palestinian women residing in ...

Polymorphism in Regulatory T-cell (Treg)-Related Genes Is Associated with Unexplained Recurrent Pregnancy Loss

Al-Ashi, Shadi F; Sharif, Fadel A.; Ashour, Mohammed J.; Badawi, Naim T. (Science Publishing Group, 2016)

In the absence of confirmed causes for around 50% of recurrent pregnancy loss (RPL) cases this study was conducted in order to investigate the association between single nucleotide polymorphism (SNP) in regulatory T-cell ...

The relationship between gene polymorphisms of coagulation factors II, V and XI and risk of recurrent pregnancy loss in Palestine

Ashour, Mohammed J.; Sharif, Fadel A. (2015)

This retrospective case-control study was carried out in order to investigate the association between Factor II (G20210A), Factor V (G1691A, H1299R, Y1702C) and Factor XI (rs3756008 A> T) gene polymorphisms and recurrent ...

Common MEFV Mutations in Palestinian Patients with Familial Mediterranean Fever

Ashour, Mohammed J.; Sharif, Fadel A. (2015)

Familial Mediterranean fever (FMF) is an autosomal recessive inflammatory disorder caused by mutations in the MEFV gene that encodes the pyrin protein. The disease is relatively common among people originating from the ...

A Novel Transglutaminase-1 Missense Mutation in a Palestinian Family with Autosomal Recessive Congenital Ichthyosis: A Case Report

Ashour, Mohammed J.; Al-Ashi, Shadi F; Sharif, Fadel A. (SCIENCEDOMAIN International, 2015)

This work presents the molecular genetics investigation of a male neonate referred to our genetics laboratory with the diagnosis of classical lamellar ichthyosis (one form of autosomal recessive congenital ichthyosis). The ...

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The single nucleotide polymorphism rs2305957 G/A is not associated with recurrent pregnancy loss

Polymorphism in Regulatory T-cell (Treg)-Related Genes Is Associated with Unexplained Recurrent Pregnancy Loss

The relationship between gene polymorphisms of coagulation factors II, V and XI and risk of recurrent pregnancy loss in Palestine

Common MEFV Mutations in Palestinian Patients with Familial Mediterranean Fever

A Novel Transglutaminase-1 Missense Mutation in a Palestinian Family with Autosomal Recessive Congenital Ichthyosis: A Case Report

Non-Syndromic autosomal recessive deafness in Gaza strip: A study of five GJB2 Gene mutations

التشوهات الكروموسومية في الذكور المعرضين مهنيا للملوثات الكيميائية في قطاع غزة - فلسطين

Chromosomal aberrations in males occupationally exposed to chemical pollutants in the gaza strip-palestine

Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip

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The single nucleotide polymorphism rs2305957 G/A is not associated with recurrent pregnancy loss

Polymorphism in Regulatory T-cell (Treg)-Related Genes Is Associated with Unexplained Recurrent Pregnancy Loss

The relationship between gene polymorphisms of coagulation factors II, V and XI and risk of recurrent pregnancy loss in Palestine

Common MEFV Mutations in Palestinian Patients with Familial Mediterranean Fever

A Novel Transglutaminase-1 Missense Mutation in a Palestinian Family with Autosomal Recessive Congenital Ichthyosis: A Case Report

Non-Syndromic autosomal recessive deafness in Gaza strip: A study of five GJB2 Gene mutations

التشوهات الكروموسومية في الذكور المعرضين مهنيا للملوثات الكيميائية في قطاع غزة - فلسطين

Chromosomal aberrations in males occupationally exposed to chemical pollutants in the gaza strip-palestine

Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip