1. Investigation of some genetic variations in BMP15 accompanied with premature ovarian failure (POF) in Syrian women
   Rana Al-ajoury et al, 2015, Middle East Fertility Society Journal CrossRef
2. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss
   Walid AL-Achkar et al, 2017, International Journal of Pediatric Otorhinolaryngology CrossRef
3. Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations
   Keita Tsukada et al, 2015, Annals of Otology, Rhinology & Laryngology CrossRef
4. GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype
   Dylan K. Chan et al, 2014, The Laryngoscope CrossRef
5. Screening ofGJB6Gene Large Deletions Among Syrians with Congenital Hearing Impairment
   Tarek Zaidieh et al, 2015, Genetic Testing and Molecular Biomarkers CrossRef
6. Genetics of hearing loss in Egypt
   Somaia Tawfik et al, 2014, Middle East Journal of Medical Genetics CrossRef
7. The OTOGL p.Arg925* Variant is Associated with Moderate Hearing Loss in a Syrian Nonconsanguineous Family
   Rana Barake et al, 2017, Genetic Testing and Molecular Biomarkers CrossRef
8. Two molecular assays for the rapid and inexpensive detection ofGJB2andGJB6mutations
   Raffaella Cascella et al, 2016, ELECTROPHORESIS CrossRef
9. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype
   WALID AL-ACHKAR et al, 2012 CrossRef
10. Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment
    Hazem Kaheel et al, 2017, Genetics Research International CrossRef
11. Molecular-cytogenetic study of de novo mosaic karyotype 45,X/46,X,i(Yq)/46,X,idic(Yq) in an azoospermic male: Case report and literature review
    Yuting Jiang et al, 2017 CrossRef
12. Investigation of the mtDNA mutations in Syrian Families With Non-Syndromic Sensorineural Hearing Loss
    Faten Moassass et al, 2018, International Journal of Pediatric Otorhinolaryngology CrossRef
13. Analysis of p.Gly12Valfs*2, p.Trp24* and p.Trp77Arg mutations in GJB2 and p.Arg81Gln variant in LRTOMT among non syndromic hearing loss Egyptian patients: implications for genetic diagnosis
    Abdullah A. Gibriel et al, 2019, Mol Biol Rep CrossRef