Elalaoui SC - Search Results

1

Natural history of non-lethal Raine syndrome during childhood.

Mameli C, Zichichi G, Mahmood N, Elalaoui SC, Mirza A, Dharmaraj P, Burrone M, Cattaneo E, Sheth J, Gandhi A, Kochar GS, Alkuraya FS, Kabra M, Mercurio G, Zuccotti G. Mameli C, et al. Among authors: elalaoui sc. Orphanet J Rare Dis. 2020 Apr 16;15(1):93. doi: 10.1186/s13023-020-01373-0. Orphanet J Rare Dis. 2020. PMID: 32299476 Free PMC article.

2

Non lethal Raine syndrome and differential diagnosis.

Elalaoui SC, Al-Sheqaih N, Ratbi I, Urquhart JE, O'Sullivan J, Bhaskar S, Williams SS, Elalloussi M, Lyahyai J, Sbihi L, Cherkaoui Jaouad I, Sbihi A, Newman WG, Sefiani A. Elalaoui SC, et al. Eur J Med Genet. 2016 Nov;59(11):577-583. doi: 10.1016/j.ejmg.2016.09.018. Epub 2016 Sep 22. Eur J Med Genet. 2016. PMID: 27667191

3

Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disorders.

Jaouad IC, Elalaoui SC, Sbiti A, Elkerh F, Belmahi L, Sefiani A. Jaouad IC, et al. Among authors: elalaoui sc. J Biosoc Sci. 2009 Sep;41(5):575-81. doi: 10.1017/S0021932009003393. Epub 2009 May 12. J Biosoc Sci. 2009. PMID: 19433002

4

Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome.

Ratbi I, Elalaoui SC, Moizard MP, Raynaud M, Sefiani A. Ratbi I, et al. Among authors: elalaoui sc. Turk J Pediatr. 2010 Sep-Oct;52(5):525-8. Turk J Pediatr. 2010. PMID: 21434539

5

A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review.

Elalaoui SC, Mariam T, Ilham R, Yassamine D, Abdelaziz S. Elalaoui SC, et al. Indian J Hum Genet. 2011 May;17(2):97-9. doi: 10.4103/0971-6866.86197. Indian J Hum Genet. 2011. PMID: 22090722 Free PMC article.

6

Severe form of hypoglossia-hypodactylia syndrome associated with complex cardiopathy: a case report.

Elalaoui SC, Ratbi I, Malih M, Bounasse M, Sefiani A. Elalaoui SC, et al. Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1092-4. doi: 10.1016/j.ijporl.2010.06.011. Epub 2010 Jul 15. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20637513

7

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A. Doubaj Y, et al. Among authors: elalaoui sc. Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991222

8

A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report.

Smaili W, Elalaoui SC, Meier S, Zerkaoui M, Sefiani A, Heinimann K. Smaili W, et al. Among authors: elalaoui sc. BMC Med Genet. 2017 May 3;18(1):50. doi: 10.1186/s12881-017-0413-8. BMC Med Genet. 2017. PMID: 28468609 Free PMC article.

9

Germline mosaicism in Rubinstein-Taybi syndrome.

Tajir M, Fergelot P, Lancelot G, Elalaoui SC, Arveiler B, Lacombe D, Sefiani A. Tajir M, et al. Among authors: elalaoui sc. Gene. 2013 Apr 15;518(2):476-8. doi: 10.1016/j.gene.2012.12.105. Epub 2013 Jan 23. Gene. 2013. PMID: 23352794

10

Novel nonsense mutation of BRCA2 gene in a Moroccan man with familial breast cancer.

Guaoua S, Ratbi I, Lyahyai J, El Alaoui SC, Laarabi FZ, Sefiani A. Guaoua S, et al. Afr Health Sci. 2014 Jun;14(2):468-71. doi: 10.4314/ahs.v14i2.25. Afr Health Sci. 2014. PMID: 25320599 Free PMC article.

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