Phenotypic spectrum and genetic analysis in the fatal cases of Schaaf-Yang syndrome
Author:
Funder
National Natural Science Foundation of China
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
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1. MAGEL2 (patho‐)physiology and Schaaf–Yang syndrome;Developmental Medicine & Child Neurology;2024-07
2. Roles of SNORD115 and SNORD116 ncRNA clusters in neuronal differentiation;2023-10-24
3. Preimplantation Genetic Testing (PGT) and Prenatal Diagnosis of Schaaf-Yang Syndrome: A Report of Three Families and a Research on Genotype–Phenotype Correlations;Journal of Clinical Medicine;2023-02-20
4. Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome;Disease Models & Mechanisms;2023-02-01
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