Publications by authors named "Imen Rejeb"

10Publications

First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations.

BMC Med Genet 2017 11 17;18(1):134. Epub 2017 Nov 17.

Service des Maladies Congénitales et Héréditaires, CHU Mongi Slim La Marsa, Sidi Daoud La Marsa, 2046, Tunis, Tunisia.

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http://dx.doi.org/10.1186/s12881-017-0493-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693559PMC
November 2017

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

Eur J Med Genet 2011 May-Jun;54(3):241-6. Epub 2011 Feb 26.

Laboratoire de Génétique Humaine, Faculté de Médecine de Tunis, 15 Jebel Lakhdhar LaRabta, Tunis 1007, Tunisia.

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http://dx.doi.org/10.1016/j.ejmg.2011.01.010DOI Listing
September 2011

Subtelomeric microduplications in three sisters with moderate mental retardation.

Biochem Genet 2010 Dec 2;48(11-12):909-14. Epub 2010 Sep 2.

Faculté de Médecine de Tunis, Laboratoire de Génétique Humaine, Tunisia.

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http://dx.doi.org/10.1007/s10528-010-9371-yDOI Listing
December 2010

X linked mental retardation.

Tunis Med 2009 May;87(5):311-8

Laboratoire de Génétique Humaine, Faculté de Médecine de Tunis, Tunisie.

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May 2009

A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features.

Eur J Hum Genet 2008 Nov 4;16(11):1358-63. Epub 2008 Jun 4.

Maladies Hereditaires et Congenitales, Service des Maladies Héréditaires et Congénitales, Hôpital Charles Nicole, Tunis, Tunisia.

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http://dx.doi.org/10.1038/ejhg.2008.103DOI Listing
November 2008