Search Results - Jehan Suleiman

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  1. 1
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    Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency by Mohamed O. E. Babiker, Manju A. Kurian, Manju A. Kurian, Jehan Suleiman, Jehan Suleiman

    Published 2022
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  2. 2
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    17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a cas... by Karen Wessel, Jehan Suleiman, Tamam E. Khalaf, Shivendra Kishore, Arndt Rolfs, Ayman W. El-Hattab

    Published 2017
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  3. 3
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    Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus by Nesreen K. Al-Jezawi, Aisha M. Al-Shamsi, Jehan Suleiman, Salma Ben-Salem, Anne John, Ranjit Vijayan, Bassam R. Ali, Lihadh Al-Gazali

    Published 2018
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