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Inesse Ben Abdallah Bouhjar

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Journal of Pediatric Genetics|September 15, 2016
Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Najla Soyah, et al.
Gene|June 25, 2013
Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardationHela Ben Khelifa, Najla Soyah, Inesse Ben-Abdallah-Bouhjar, et al.
Journal of Pediatric Genetics|September 15, 2016
Cytogenetic analysis in a large series of children with non-syndromic mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Soumaya Mougou-Zrelli, et al.
Gene|February 14, 2013
Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literatureInesse Ben-Abdallah-Bouhjar, Soumya Mougou-Zerelli, Hanene Hannachi, et al.
European Journal of Medical Genetics|June 12, 2012
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotoniaInesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Array-CGH study of partial trisomy 9p without mental retardationInesse Ben Abdallah Bouhjar, Hanane Hannachi, Soumaya Mougou Zerelli, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Pediatric Genetics|September 15, 2016
Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Najla Soyah, et al.
Gene|June 25, 2013
Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardationHela Ben Khelifa, Najla Soyah, Inesse Ben-Abdallah-Bouhjar, et al.
Journal of Pediatric Genetics|September 15, 2016
Cytogenetic analysis in a large series of children with non-syndromic mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Soumaya Mougou-Zrelli, et al.
Gene|February 14, 2013
Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literatureInesse Ben-Abdallah-Bouhjar, Soumya Mougou-Zerelli, Hanene Hannachi, et al.
European Journal of Medical Genetics|June 12, 2012
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotoniaInesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Array-CGH study of partial trisomy 9p without mental retardationInesse Ben Abdallah Bouhjar, Hanane Hannachi, Soumaya Mougou Zerelli, et al.
Pageof 1