Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34
Author:
Publisher
Frontiers Media SA
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference26 articles.
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1. X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review;Molecular Genetics and Metabolism Reports;2024-03
2. Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome;BMC Medical Genomics;2024-01-18
3. A novel NONO nonsense variant in a fetus with renal abnormalities;Prenatal Diagnosis;2023-12-18
4. Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder;Frontiers in Genetics;2023-07-18
5. Current status and challenges in prenatal and neonatal screening, diagnosis, and management of congenital heart disease in China;The Lancet Child & Adolescent Health;2023-07
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