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Community genetics. Its definition 2010.
Ten Kate LP, Al-Gazali L, Anand S, Bittles A, Cassiman JJ, Christianson A, Cornel MC, Hamamy H, Kääriäinen H, Kristoffersson U, Marais D, Penchaszadeh VB, Rahman P, Schmidtke J. Ten Kate LP, et al. Among authors: hamamy h. J Community Genet. 2010 Mar;1(1):19-22. doi: 10.1007/s12687-010-0007-z. Epub 2010 Mar 31. J Community Genet. 2010. PMID: 21475671 Free PMC article.
Consanguinity and dysmorphology in Arabs.
Al-Gazali L, Hamamy H. Al-Gazali L, et al. Among authors: hamamy h. Hum Hered. 2014;77(1-4):93-107. doi: 10.1159/000360421. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060273 Free article.
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide.
Blencowe H, Moorthie S, Petrou M, Hamamy H, Povey S, Bittles A, Gibbons S, Darlison M, Modell B; Congenital Disorders Expert Group. Blencowe H, et al. Among authors: hamamy h. J Community Genet. 2018 Oct;9(4):397-406. doi: 10.1007/s12687-018-0376-2. Epub 2018 Aug 14. J Community Genet. 2018. PMID: 30109643 Free PMC article.
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.
Moorthie S, Blencowe H, Darlison MW, Lawn J, Morris JK, Modell B; Congenital Disorders Expert Group; Bittles AH, Blencowe H, Christianson A, Cousens S, Darlison MW, Gibbons S, Hamamy H, Khoshnood B, Howson CP, Lawn J, Mastroiacovo P, Modell B, Moorthie S, Morris JK, Mossey PA, Neville AJ, Petrou M, Povey S, Rankin J, Schuler-Faccini L, Wren C, Yunnis KA. Moorthie S, et al. Among authors: hamamy h. J Community Genet. 2018 Oct;9(4):387-396. doi: 10.1007/s12687-018-0384-2. Epub 2018 Sep 14. J Community Genet. 2018. PMID: 30218347 Free PMC article.
Genetic disorders in the Arab world.
Al-Gazali L, Hamamy H, Al-Arrayad S. Al-Gazali L, et al. Among authors: hamamy h. BMJ. 2006 Oct 21;333(7573):831-4. doi: 10.1136/bmj.38982.704931.AE. BMJ. 2006. PMID: 17053236 Free PMC article. Review. No abstract available.
Jordan: communities and community genetics.
Hamamy H, Al-Hait S, Alwan A, Ajlouni K. Hamamy H, et al. Community Genet. 2007;10(1):52-60. doi: 10.1159/000096282. Community Genet. 2007. PMID: 17167252
Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Schmidt-von Kegler M, Merriman B, Nelson SF, Masri A, Alkazaleh F, Guerra D, Ferrari P, Nanda A, Rajab A, Markie D, Gray M, Nelson J, Grix A, Sommer A, Savarirayan R, Janecke AR, Steichen E, Sillence D, Hausser I, Budde B, Nürnberg G, Nürnberg P, Seemann P, Kunkel D, Zambruno G, Dallapiccola B, Schuelke M, Robertson S, Hamamy H, Wollnik B, Van Maldergem L, Mundlos S, Kornak U. Reversade B, et al. Among authors: hamamy h. Nat Genet. 2009 Sep;41(9):1016-21. doi: 10.1038/ng.413. Epub 2009 Aug 2. Nat Genet. 2009. PMID: 19648921
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report.
Hamamy H, Antonarakis SE, Cavalli-Sforza LL, Temtamy S, Romeo G, Kate LP, Bennett RL, Shaw A, Megarbane A, van Duijn C, Bathija H, Fokstuen S, Engel E, Zlotogora J, Dermitzakis E, Bottani A, Dahoun S, Morris MA, Arsenault S, Aglan MS, Ajaz M, Alkalamchi A, Alnaqeb D, Alwasiyah MK, Anwer N, Awwad R, Bonnefin M, Corry P, Gwanmesia L, Karbani GA, Mostafavi M, Pippucci T, Ranza-Boscardin E, Reversade B, Sharif SM, Teeuw ME, Bittles AH. Hamamy H, et al. Genet Med. 2011 Sep;13(9):841-7. doi: 10.1097/GIM.0b013e318217477f. Genet Med. 2011. PMID: 21555946 Free article.
97 results