Maazoul F - Search Results

1

Neonatal death in Marshall-Smith syndrome.

Chatel C, Maazoul F, Sigaudy S, Fredouille C, Ayme S, Philip N. Chatel C, et al. Among authors: maazoul f. Genet Couns. 1998;9(1):15-8. Genet Couns. 1998. PMID: 9555581

2

DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE.

Attig A, Ben Jemaa L, Kraoua L, Jilani H, Maazoul F, Mrad R. Attig A, et al. Among authors: maazoul f. Genet Couns. 2016;27(3):441-446. Genet Couns. 2016. PMID: 30204977 No abstract available.

3

OCULO-DENTO-DIGITAL DYSPLASIA IN A TUNISIAN FAMILY WITH A NOVEL GJA1 MUTATION.

Attig A, Trabelsi M, Hizem S, Ben Jemaa L, Maazoul F, Chaouachi S, Mrad R. Attig A, et al. Among authors: maazoul f. Genet Couns. 2016;27(3):433-439. Genet Couns. 2016. PMID: 30204976 No abstract available.

4

[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: maazoul f. Tunis Med. 2007 Oct;85(10):885-90. Tunis Med. 2007. PMID: 18236814 French.

5

[Genetic analysis of Turner syndrome: 89 cases in Tunisia].

Kammoun I, Chaabouni M, Trabelsi M, Ouertani I, Kraoua L, Chelly I, M'rad R, Ben Jemaa L, Maâzoul F, Chaabouni H. Kammoun I, et al. Among authors: maazoul f. Ann Endocrinol (Paris). 2008 Nov;69(5):440-5. doi: 10.1016/j.ando.2008.01.007. Epub 2008 Jun 9. Ann Endocrinol (Paris). 2008. PMID: 18541220 French.

6

[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: maazoul f. Tunis Med. 1999 Aug-Sep;77(8-9):407-14. Tunis Med. 1999. PMID: 10611817 French. No abstract available.

7

Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.

Kraoua L, Chaabouni M, Ewers E, Chelly I, Ouertani I, Ben Jemaa L, Maazoul F, Liehr T, Chaabouni H. Kraoua L, et al. Among authors: maazoul f. Eur J Med Genet. 2011 Jul-Aug;54(4):e446-50. doi: 10.1016/j.ejmg.2011.04.007. Epub 2011 May 6. Eur J Med Genet. 2011. PMID: 21621018

8

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: maazoul f. 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

9

Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V.

Kharrat M, Trabelsi S, Chaabouni M, Maazoul F, Kraoua L, Ben Jemaa L, Gandoura N, Barsaoui S, Morel Y, M'rad R, Chaabouni H. Kharrat M, et al. Among authors: maazoul f. Clin Genet. 2010 Oct;78(4):398-401. doi: 10.1111/j.1399-0004.2010.01403.x. Clin Genet. 2010. PMID: 20331679

10

[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: maazoul f. Tunis Med. 1998 May;76(5):113-9. Tunis Med. 1998. PMID: 9739203 Review. French. No abstract available.

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