Jehan Suleiman
8PUBLICATIONS
17CO-AUTHORS
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Publications (8)
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|Mar 17, 2023
Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review.Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi
|Dec 20, 2022
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy.Shuk Ching Chong, Ye Cao, Eva L W Fung
|May 05, 2022
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency.Korbinian M Riedhammer, Anna L Burgemeister, Vincent Cantagrel
|Dec 18, 2019
VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features.Christian Beetz, Najim Ameziane, Ameni Kdissa
|May 30, 2018
PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities.J Suleiman, A M Al Hashem, B Tabarki
|Apr 11, 2018
TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies.J Suleiman, M Mundt, S Sampath
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Frequent Collaborators
6 joint publications
Ayman W El-Hattab
1 joint publications
F S Alkuraya
1 joint publications
K Al-Thihli
1 joint publications
Christian Beetz
1 joint publications
Peter Bauer
1 joint publications
Korbinian M Riedhammer
1 joint publications
Vincent Cantagrel
1 joint publications
Patricia L Kannouche
1 joint publications
Anne M Slavotinek
1 joint publications
Rosanna Weksberg
