Dahoun S - Search Results

1

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. Among authors: dahoun s. Genet Med. 2011 Sep;13(9):841-7. doi: 10.1097/GIM.0b013e318217477f. Genet Med. 2011. PMID: 21555946 Free article.

2

Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?

Makrythanasis P, Gimelli S, Béna F, Dahoun S, Morris MA, Antonarakis SE, Bottani A. Makrythanasis P, et al. Among authors: dahoun s. Eur J Med Genet. 2012 Jan;55(1):63-6. doi: 10.1016/j.ejmg.2011.11.001. Epub 2011 Nov 10. Eur J Med Genet. 2012. PMID: 22080113

3

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

Glaser B, Debbane M, Hinard C, Morris MA, Dahoun SP, Antonarakis SE, Eliez S. Glaser B, et al. Among authors: dahoun sp. Am J Psychiatry. 2006 Mar;163(3):537-9. doi: 10.1176/appi.ajp.163.3.537. Am J Psychiatry. 2006. PMID: 16513880

4

Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events.

Dahoun S, Gagos S, Gagnebin M, Gehrig C, Burgi C, Simon F, Vieux C, Extermann P, Lyle R, Morris MA, Antonarakis SE, Béna F, Blouin JL. Dahoun S, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2086-93. doi: 10.1002/ajmg.a.32431. Am J Med Genet A. 2008. PMID: 18627064

5

A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis.

Paoloni-Giacobino A, Dutoit MH, Morris MA, Dahoun SP. Paoloni-Giacobino A, et al. Among authors: dahoun sp. Clin Genet. 1999 Apr;55(4):256-8. doi: 10.1034/j.1399-0004.1999.550407.x. Clin Genet. 1999. PMID: 10361986

6

Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.

Martinet D, Filges I, Besuchet Schmutz N, Morris MA, Gaide AC, Dahoun S, Bottani A, Addor MC, Antonarakis SE, Beckmann JS, Béna F. Martinet D, et al. Among authors: dahoun s. Am J Med Genet A. 2008 Aug 15;146A(16):2094-102. doi: 10.1002/ajmg.a.32414. Am J Med Genet A. 2008. PMID: 18629875

7

A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features.

Béna F, Bottani A, Marcelli F, Sizonenko LD, Conrad B, Dahoun S. Béna F, et al. Among authors: dahoun s. Am J Med Genet A. 2007 Aug 15;143A(16):1894-9. doi: 10.1002/ajmg.a.31789. Am J Med Genet A. 2007. PMID: 17632785

8

Parental decisions following the prenatal diagnosis of sex chromosome abnormalities.

Hamamy HA, Dahoun S. Hamamy HA, et al. Among authors: dahoun s. Eur J Obstet Gynecol Reprod Biol. 2004 Sep 10;116(1):58-62. doi: 10.1016/j.ejogrb.2003.12.029. Eur J Obstet Gynecol Reprod Biol. 2004. PMID: 15294369

9

Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility.

Paoloni-Giacobino A, Kern I, Rumpler Y, Djlelati R, Morris MA, Dahoun SP. Paoloni-Giacobino A, et al. Among authors: dahoun sp. Clin Genet. 2000 Oct;58(4):324-8. doi: 10.1034/j.1399-0004.2000.580411.x. Clin Genet. 2000. PMID: 11076058

10

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.

Lyle R, Béna F, Gagos S, Gehrig C, Lopez G, Schinzel A, Lespinasse J, Bottani A, Dahoun S, Taine L, Doco-Fenzy M, Cornillet-Lefèbvre P, Pelet A, Lyonnet S, Toutain A, Colleaux L, Horst J, Kennerknecht I, Wakamatsu N, Descartes M, Franklin JC, Florentin-Arar L, Kitsiou S, Aït Yahya-Graison E, Costantine M, Sinet PM, Delabar JM, Antonarakis SE. Lyle R, et al. Among authors: dahoun s. Eur J Hum Genet. 2009 Apr;17(4):454-66. doi: 10.1038/ejhg.2008.214. Epub 2008 Nov 12. Eur J Hum Genet. 2009. PMID: 19002211 Free PMC article.

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