Dahoun S - Search Results

1

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

2

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.

3

[Anomalies of sex chromosomes in amniocentesis].

Paoloni-Giacobino A, Dahoun S, Hamany H, Lespinasse J. Paoloni-Giacobino A, et al. Among authors: dahoun s. Rev Med Suisse Romande. 2004 Mar;124(3):167-9. Rev Med Suisse Romande. 2004. PMID: 15095663 French.

4

[A second case of (de novo) paracentric inversion of the short arm of the X chromosome].

Dahoun S. Dahoun S. Ann Genet. 1990;33(1):52-5. Ann Genet. 1990. PMID: 2195983 Review. French.

5

Initiation of a medical genetics service in sub-Saharan Africa: experience of prenatal diagnosis in Cameroon.

Wonkam A, Tekendo CN, Sama DJ, Zambo H, Dahoun S, Béna F, Morris MA. Wonkam A, et al. Among authors: dahoun s. Eur J Med Genet. 2011 Jul-Aug;54(4):e399-404. doi: 10.1016/j.ejmg.2011.03.013. Epub 2011 Apr 5. Eur J Med Genet. 2011. PMID: 21473937

6

No association between DUP25 and anxiety disorders.

Henrichsen CN, Delorme R, Boucherie M, Marelli D, Baud P, Bellivier F, Courtet P, Chabane N, Henry C, Leboyer M, Malafosse A, Antonarakis SE, Dahoun S. Henrichsen CN, et al. Among authors: dahoun s. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):80-3. doi: 10.1002/ajmg.b.30037. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211637

7

A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH.

Paoloni-Giacobino A, Lespinasse J, Moix I, Dahoun SP. Paoloni-Giacobino A, et al. Among authors: dahoun sp. Ann Genet. 2001 Jul-Sep;44(3):117-9. doi: 10.1016/s0003-3995(01)01086-3. Ann Genet. 2001. PMID: 11694221

8

Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocation.

Paoloni-Giacobino A, Bottani A, Dahoun SP. Paoloni-Giacobino A, et al. Among authors: dahoun sp. Ann Genet. 1999;42(3):166-9. Ann Genet. 1999. PMID: 10526660

9

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

10

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

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