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Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.
Abdel-Salam GMH, Sayed ISM, Afifi HH, Abdel-Ghafar SF, Abouzaid MR, Ismail SI, Aglan MS, Issa MY, El-Bassyouni HT, El-Kamah G, Effat LK, Eid M, Zaki MS, Temtamy SA, Abdel-Hamid MS. Abdel-Salam GMH, et al. Am J Med Genet A. 2020 Jun;182(6):1407-1420. doi: 10.1002/ajmg.a.61585. Epub 2020 Apr 8. Am J Med Genet A. 2020. PMID: 32267100
The most encountered groups of genetic disorders in Giza Governorate, Egypt.
Afifi HH, El-Ruby MO, El-Bassyouni HT, Ismail SI, Aglan MS, El-Harouni AA, Mazen IM, Zaki MS, Bassiouni RI, Hosny LA, El-Kamah GY, El-Kotoury AI, Ashour AM, Abdel-Salam GM, El-Gammal MA, Hamed K, Kamal RM, El-Nekhely I, Temtamy SA. Afifi HH, et al. Bratisl Lek Listy. 2010;111(2):62-9. Bratisl Lek Listy. 2010. PMID: 20429316
Growth curves of Egyptian patients with Turner syndrome.
El-Bassyouni HT, Afifi HH, Aglan MS, Mahmoud WM, Zaki ME. El-Bassyouni HT, et al. Am J Med Genet A. 2012 Nov;158A(11):2687-91. doi: 10.1002/ajmg.a.35518. Epub 2012 Jul 27. Am J Med Genet A. 2012. PMID: 22847945
Anti-diuretic hormone and genetic study in primary nocturnal enuresis.
Fatouh AA, Motawie AA, Abd Al-Aziz AM, Hamed HM, Awad MA, El-Ghany AA, El Bassyouni HT, Shehab MI, Eid MM. Fatouh AA, et al. J Pediatr Urol. 2013 Dec;9(6 Pt A):831-7. doi: 10.1016/j.jpurol.2012.11.009. Epub 2012 Dec 14. J Pediatr Urol. 2013. PMID: 23246575
Ring chromosome 15: expanding the phenotype.
Eid MM, El-Bassyouni HT, Eid OM, Hamad SA, Elgerzawy A, Zaki MS, El-Ruby M. Eid MM, et al. Genet Couns. 2013;24(4):417-25. Genet Couns. 2013. PMID: 24551985
55 results