Ben Jemaa L - Search Results

1

A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation.

Rejeb I, Ben Jemaa L, Abaied L, Kraoua L, Saillour Y, Maazoul F, Chelly J, Chaabouni H. Rejeb I, et al. Among authors: ben jemaa l. Eur J Med Genet. 2011 May-Jun;54(3):241-6. doi: 10.1016/j.ejmg.2011.01.010. Epub 2011 Feb 26. Eur J Med Genet. 2011. PMID: 21315190

2

[Cytogenetic study of 500 patients selected in the research for chromosomal anomalies].

Chaabouni H, Meddeb M, Buresi C, Ben Jemaa L. Chaabouni H, et al. Among authors: ben jemaa l. Tunis Med. 1992 Jan;70(1):39-43. Tunis Med. 1992. PMID: 1570651 French. No abstract available.

3

[Value and practical applications of cytogenetic in situ hybridization technique].

Hila L, Ben Jemaa L, Mrad R, Maazoul F, Chaabouni H. Hila L, et al. Among authors: ben jemaa l. Tunis Med. 1998 May;76(5):113-9. Tunis Med. 1998. PMID: 9739203 Review. French. No abstract available.

4

[Epidemiologic and genetic study of trisomy 21 in Tunisia].

Chaabouni H, Smaoui N, Maazoul F, Ben Jemaa L, M'Rad R. Chaabouni H, et al. Among authors: ben jemaa l. Tunis Med. 1999 Aug-Sep;77(8-9):407-14. Tunis Med. 1999. PMID: 10611817 French. No abstract available.

5

Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.

Mrad R, Dorboz I, Ben Jemaa L, Maazoul F, Trabelsi M, Chaabouni M, Mlaiki B, Miladi N, Hentati F, Chaabouni H. Mrad R, et al. Among authors: ben jemaa l. Tunis Med. 2006 Aug;84(8):465-9. Tunis Med. 2006. PMID: 17175684

6

MEFV mutations in Tunisian patients suffering from familial Mediterranean fever.

Chaabouni HB, Ksantini M, M'rad R, Kharrat M, Chaabouni M, Maazoul F, Bahloul Z, Ben Jemaa L, Ben Moussa F, Ben Chaabane T, Mrad S, Touitou I, Smaoui N. Chaabouni HB, et al. Among authors: ben moussa f, ben jemaa l, ben chaabane t. Semin Arthritis Rheum. 2007 Jun;36(6):397-401. doi: 10.1016/j.semarthrit.2006.12.004. Epub 2007 Feb 5. Semin Arthritis Rheum. 2007. PMID: 17276496

7

Y chromosome microdeletions in Tunisian infertile males.

Rejeb I, M'rad R, Maazoul F, Trabelsi M, Ben Jemaa L, Chaabouni M, Zhioua F, Chaabouni H. Rejeb I, et al. Among authors: ben jemaa l. Pathol Biol (Paris). 2008 May;56(3):111-5. doi: 10.1016/j.patbio.2007.05.002. Epub 2007 Nov 26. Pathol Biol (Paris). 2008. PMID: 18031951

8

[Treacher-Collins syndrome: clinical and genetic aspects apropos of 4 cases of which 1 is familial].

Chaabouni M, Fersi M, Belghith N, Maazoul F, M'rad R, Ben Jemaa L, Gandoura N, Chaabouni H. Chaabouni M, et al. Among authors: ben jemaa l. Tunis Med. 2007 Oct;85(10):885-90. Tunis Med. 2007. PMID: 18236814 French.

9

De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.

Bayou N, M'rad R, Belhaj A, Daoud H, Ben Jemaa L, Zemni R, Briault S, Helayem MB, Chaabouni H. Bayou N, et al. Among authors: ben jemaa l. J Biomed Biotechnol. 2008;2008:231904. doi: 10.1155/2008/231904. J Biomed Biotechnol. 2008. PMID: 18475318 Free PMC article.

10

The creatine transporter gene paralogous at 16p11.2 is expressed in human brain.

Bayou N, M'rad R, Belhaj A, Daoud H, Zemni R, Briault S, Helayem MB, Ben Jemaa L, Chaabouni H. Bayou N, et al. Among authors: ben jemaa l. Comp Funct Genomics. 2008;2008:609684. doi: 10.1155/2008/609684. Comp Funct Genomics. 2008. PMID: 18509488 Free PMC article.

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

33 results

Search Page

Filters