Sbiti A - Search Results

1

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Amasdl S, Natiq A, Elalaoui SC, Sbiti A, Liehr T, Sefiani A. Amasdl S, et al. Among authors: sbiti a. J Med Case Rep. 2016 May 13;10(1):122. doi: 10.1186/s13256-016-0830-x. J Med Case Rep. 2016. PMID: 27178284 Free PMC article.

2

A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.

Deqaqi SC, N'Guessan M, Forner J, Sbiti A, Beldjord C, Chelly J, Sefiani A, Des Portes V. Deqaqi SC, et al. Among authors: sbiti a. Ann Genet. 1998;41(1):11-6. Ann Genet. 1998. PMID: 9599645

3

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients.

Sbiti A, El Kerch F, Sefiani A. Sbiti A, et al. J Biomed Biotechnol. 2002;2(3):158-160. doi: 10.1155/S1110724302205069. J Biomed Biotechnol. 2002. PMID: 12488581 Free PMC article.

4

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.

Baala L, Briault S, Etchevers HC, Laumonnier F, Natiq A, Amiel J, Boddaert N, Picard C, Sbiti A, Asermouh A, Attié-Bitach T, Encha-Razavi F, Munnich A, Sefiani A, Lyonnet S. Baala L, et al. Among authors: sbiti a. Nat Genet. 2007 Apr;39(4):454-6. doi: 10.1038/ng1993. Epub 2007 Mar 11. Nat Genet. 2007. PMID: 17353897

5

Unexpected fertility and paternal UPD 22.

Ouldim K, Sbiti A, Natiq A, El-Kerch F, Cherkaoui S, Sefiani A. Ouldim K, et al. Among authors: sbiti a. Fertil Steril. 2008 Nov;90(5):2013.e13-5. doi: 10.1016/j.fertnstert.2008.03.067. Epub 2008 Jun 20. Fertil Steril. 2008. PMID: 18571167 Free article.

6

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: sbiti a. J Biosoc Sci. 2009 Sep;41(5):575-81. doi: 10.1017/S0021932009003393. Epub 2009 May 12. J Biosoc Sci. 2009. PMID: 19433002

7

Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases.

Jaouad IC, Cherkaoui Deqaqi S, Sbiti A, Natiq A, Elkerch F, Sefiani A. Jaouad IC, et al. Among authors: sbiti a. Singapore Med J. 2010 Feb;51(2):133-6. Singapore Med J. 2010. PMID: 20358152 Free article.

8

Spinal muscular atrophy carrier frequency and estimated prevalence of the disease in Moroccan newborns.

Lyahyai J, Sbiti A, Barkat A, Ratbi I, Sefiani A. Lyahyai J, et al. Among authors: sbiti a. Genet Test Mol Biomarkers. 2012 Mar;16(3):215-8. doi: 10.1089/gtmb.2011.0149. Epub 2011 Sep 27. Genet Test Mol Biomarkers. 2012. PMID: 21950724

9

[Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco].

Sbiti A, Ratbi I, Kriouile Y, Sefiani A. Sbiti A, et al. Arch Pediatr. 2011 Dec;18(12):1261-4. doi: 10.1016/j.arcped.2011.09.025. Epub 2011 Oct 29. Arch Pediatr. 2011. PMID: 22041598 French.

10

Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco.

Aboussair N, Jaouad IC, Dequaqui SC, Sbiti A, Elkerch F, Yahya B, Natiq A, Sefiani A. Aboussair N, et al. Among authors: sbiti a. Genet Test Mol Biomarkers. 2012 Jun;16(6):569-73. doi: 10.1089/gtmb.2011.0265. Epub 2012 Apr 16. Genet Test Mol Biomarkers. 2012. PMID: 22506488

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

20 results

Search Page

Filters