Dahoun S - Search Results

1

Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.

Migliore C, Athanasakis E, Dahoun S, Wonkam A, Lees M, Calabrese O, Connell F, Lynch SA, Izzi C, Pompilii E, Thakur S, van Maarle M, Wilson LC, Meroni G. Migliore C, et al. Among authors: dahoun s. Eur J Med Genet. 2013 Aug;56(8):404-10. doi: 10.1016/j.ejmg.2013.05.009. Epub 2013 Jun 19. Eur J Med Genet. 2013. PMID: 23791568

2

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

3

MECP2 duplication syndrome in a patient from Cameroon.

Tekendo-Ngongang C, Dahoun S, Nguefack S, Moix I, Gimelli S, Zambo H, Morris MA, Sloan-Béna F, Wonkam A. Tekendo-Ngongang C, et al. Among authors: dahoun s. Am J Med Genet A. 2020 Apr;182(4):619-622. doi: 10.1002/ajmg.a.61510. Epub 2020 Feb 13. Am J Med Genet A. 2020. PMID: 32052928 Free PMC article.

4

The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.

Wonkam A, Toko R, Chelo D, Tekendo-Ngongang C, Kingue S, Dahoun S. Wonkam A, et al. Among authors: dahoun s. Glob Heart. 2017 Jun;12(2):115-120. doi: 10.1016/j.gheart.2017.01.003. Epub 2017 Mar 13. Glob Heart. 2017. PMID: 28302550 Free article.

5

Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.

Tekendo-Ngongang C, Dahoun S, Nguefack S, Gimelli S, Sloan-Béna F, Wonkam A. Tekendo-Ngongang C, et al. Among authors: dahoun s. Mol Syndromol. 2014 Dec;5(6):287-92. doi: 10.1159/000369421. Epub 2014 Nov 29. Mol Syndromol. 2014. PMID: 25565928 Free PMC article.

6

Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon.

Wonkam A, Zambo H, Tekendo CN, Béna F, Dahoun S. Wonkam A, et al. Among authors: dahoun s. Int J Gynaecol Obstet. 2012 Feb;116(2):174-5. doi: 10.1016/j.ijgo.2011.10.006. Epub 2011 Nov 9. Int J Gynaecol Obstet. 2012. PMID: 22078054 No abstract available.

7

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

8

An excess of chromosome 1 breakpoints in male infertility.

Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N. Bache I, et al. Among authors: dahoun s. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911

9

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

10

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

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