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S. Mougou-Zerelli
S. Mougou-Zerelli
Lissencephaly
Monosomy
PAFAH1B1
Chromosome 21
Karyotype
2
Papers
7
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0
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Élargissement du spectre phénotypique du syndrome meds (microcéphalie, épilepsie et diabète néonatal) lié au gène IER3IP1 : à propos d’un cas Tunisien présentant un hypogonadisme
2020
Annales D Endocrinologie
K. Rjiba
N. Soyah
Molka Kammoun
I. Hadj Hmida
Ali Saad
Ken McElreavey
S. Mougou-Zerelli
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Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man.
2011
Cytogenetic and Genome Research
Hanene Hannachi
S. Mougou-Zerelli
I. Benabdallah
N. Mama
I Hamdi
Audrey Labalme
H. Elghezal
Damien Sanlaville
Ali Saad
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Citations (7)
1