Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype-Genotype Correlation in 97 Patients with Motor Developmental Delay.

Autor: Belghiti HD; Medical Center of Biomedical and Translational Research, Hassan II University Hospital, Fez, Morocco., Abbassi M; Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, Fez, Morocco., Sayel H; Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, Fez, Morocco., Ahakoud M; Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, Fez, Morocco., El Makhzen BE; Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, Fez, Morocco., Lee N; Department of Pharmacology and Physiology, The George Washington University School of Medicine and Health Sciences, Washington, United States., Russo S; Istituto Auxologico Italiano Istituto di Ricovero e Cura a Carattere Scientifico, Cytogenetics and Molecular Genetics Laboratory, Milano, Lombardia, Italy., Chaouki S; Department of Neuropediatrics, Hospital University Hassan II, Fez, Morocco., Bouguenouch L; Unit of Medical Genetics and Oncogenetics, University Hospital Hassan II, Fez, Morocco.

Publikováno v: Journal of pediatric genetics [J Pediatr Genet] 2022 Aug 16; Vol. 13 (1), pp. 15-21. Date of Electronic Publication: 2022 Aug 16 (Print Publication: 2024).