Muenke syndrome Addissie, Yonit A.; Yarnell, Colin M.P.; Kruszka, Paul; More Addissie, Yonit A.; Yarnell, Colin M.P.; Kruszka, Paul; Muenke, Maximilian Less Middle East Journal of Medical Genetics. 4(1):1-6, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation Aglan, Mona S.; Abdel-Hamid, Mohamed S.; Otaify, Ghada A.; More Aglan, Mona S.; Abdel-Hamid, Mohamed S.; Otaify, Ghada A.; Ismail, Somaia M.; Effat, Laila K.; Temtamy, Samia A. Less Middle East Journal of Medical Genetics. 4(1):7-12, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia Eid, Maha M.; Abdel-Messih, Ibrahim Y.; El-Kamah, Ghada Y.; More Eid, Maha M.; Abdel-Messih, Ibrahim Y.; El-Kamah, Ghada Y.; Mahmoud, Hanan M.; Shihab, Marwa I.; El-Azhary, Nermeen H. Less Middle East Journal of Medical Genetics. 4(1):13-17, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis Temtamy, Samia A.; Aglan, Mona S.; Otaify, Ghada A.; More Temtamy, Samia A.; Aglan, Mona S.; Otaify, Ghada A.; Abdel-Hamid, Mohamed; Ismail, Somaia; Makrythanasis, Periklis; Hamamy, Hanan; Antonarakis, Stylianos E. Less Middle East Journal of Medical Genetics. 4(1):18-23, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
A rare case of isochromosome 10: i(10p) and i(10q) Elbastawisy, Hanan I.; Ghaly, Samuel W.; Abualhasan, Sawsan J. Elbastawisy, Hanan I.; Ghaly, Samuel W.; Abualhasan, Sawsan J. Less Middle East Journal of Medical Genetics. 4(1):24-27, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
A case report of FATCO syndrome: fibular aplasia, tibial campomelia, and oligosyndactyly Bastaki, Laila A.; Al-Hathal, Muneef; Sadik, Doaa I.; More Bastaki, Laila A.; Al-Hathal, Muneef; Sadik, Doaa I.; Alrohaif, Hadil E.; Yousef, Hala Y.; Khallaf, Mohamed G. Less Middle East Journal of Medical Genetics. 4(1):28-30, January 2015. Abstract Abstract Favorites PDF Get Content & Permissions Go to Full Text of this Article Free
