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A case of de novo trisomy 12p syndrome.
Tayel S, McCorquodale MM, Rutherford T, Kurczynski TW, Abdel-Aziz AM, el-Gabaldy F, Sharaf EA. Tayel S, et al. Clin Genet. 1989 May;35(5):382-6. doi: 10.1111/j.1399-0004.1989.tb02958.x. Clin Genet. 1989. PMID: 2758689
Triophthalmia and facial clefting: a case report.
Tayel SM, Sabry MA, Kader NA, Farah S, Al-Awadi SA, Farag TI. Tayel SM, et al. J Med Genet. 1998 Oct;35(10):875-7. doi: 10.1136/jmg.35.10.875. J Med Genet. 1998. PMID: 9783717 Free PMC article.
Trisomy 18 in Kuwait.
Naguib KK, Al-Awadi SA, Moussa MA, Bastaki L, Gouda S, Redha MA, Mustafa F, Tayel SM, Abulhassan SA, Murthy DS. Naguib KK, et al. Among authors: tayel sm. Int J Epidemiol. 1999 Aug;28(4):711-6. doi: 10.1093/ije/28.4.711. Int J Epidemiol. 1999. PMID: 10480700 Clinical Trial.
Mosaic Turner syndrome: cytogenetics versus FISH.
Abulhasan SJ, Tayel SM, al-Awadi SA. Abulhasan SJ, et al. Among authors: tayel sm. Ann Hum Genet. 1999 May;63(Pt 3):199-206. doi: 10.1046/j.1469-1809.1999.6330199.x. Ann Hum Genet. 1999. PMID: 10738532
A morpho-etiological description of congenital limb anomalies.
Tayel SM, Fawzia MM, Al-Naqeeb NA, Gouda S, Al Awadi SA, Naguib KK. Tayel SM, et al. Ann Saudi Med. 2005 May-Jun;25(3):219-27. doi: 10.5144/0256-4947.2005.219. Ann Saudi Med. 2005. PMID: 16119523 Free PMC article.
76 results