Showing 1 - 2 results of 2 for search 'Yahya Benbouchta', query time: 0.08s Refine Results
  1. 1
    15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review

    15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review by Yahya Benbouchta, Nicole De Leeuw, Saadia Amasdl, Aziza Sbiti, Dominique Smeets, Khalid Sadki, Abdelaziz Sefiani

    Published 2021-09-01
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    Article
  2. 2
    Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

    Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report by Yahya Benbouchta, Imane Cherkaoui Jaouad, Habiba Tazi, Hamza Elorch, Mouna Ouhenach, Abdelali Zrhidri, Khalid Sadki, Abdelaziz Sefiani, Jaber Lyahyai, Amina Berraho

    Published 2021-01-01
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