Najla Soyah

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia

Inesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme et al. · European Journal of Medical Genetics · 2012 · 44 citations

Life Sciences, Genetics, Molecular Genetics +13

Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation

Hela Ben Khelifa, Najla Soyah, Inesse Ben-Abdallah-Bouhjar et al. · Gene · 2013 · 42 citations

Life Sciences, Genetics, Molecular Genetics +17

Array‐CGH study of partial trisomy 9p without mental retardation

Inesse Ben Abdallah Bouhjar, Hanane Hannachi, Soumaya Mougou Zerelli et al. · American Journal of Medical Genetics Part A · 2011 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients.

Inesse Ben Abdallah-Bouhjar, Soumaya Mougou-Zerelli, Hanene Hannachi et al. · PubMed · 2013 · 11 citations

Life Sciences, Genetics, Molecular Genetics +17

Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case

Khouloud Rjiba, Najla Soyah, Molka Kammoun et al. · European Journal of Medical Genetics · 2021 · 10 citations

Life Sciences, Molecular Medicine, Neurology +7