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

Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease

by Abdelali Zrhidri, Saadia Amasdl, Jaber Lyahyai, Hanane Elouardi, Bouchra Chkirate, Laure Raymond, Grégory Egéa, Mohamed Taoudi, Said El Mouatassim, Abdelaziz Sefiani
Published 2017-09-01