Associated Papers
NONO-Related Syndromic X-Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort.
Zhao Y et al.
Prenatal Diagnosis, 2026
Identification of a novel de novo NONO variants causing X-linked syndromic intellectual developmental disorder-34 in a fetus.
Huang R et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2026
Case Report: A female case of X-linked intellectual disability syndrome type 34 caused by a NONO frameshift variant and literature review.
Zhang Y et al.
Frontiers in Pediatrics, 2026
Are NONO variants linked to congenital heart disease? Patient reports and review.
He P et al.
European Journal of Medical Genetics, 2025
X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review.
Xi H et al.
Molecular Genetics and Metabolism Reports, 2024
[Identification of a NONO gene variant in a child with congenital heart disease and global developmental delay].
Lei Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2023
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Roessler F et al.
American Journal of Medical Genetics. Part A, 2023
Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease.
Tan M et al.
Frontiers in Genetics, 2022
35910219 (PubMed )
Supplement: DataSheet1.xlsx › Table_S2
Not Only Diagnostic Yield: Whole-Exome Sequencing in Infantile Cardiomyopathies Impacts on Clinical and Family Management.
Pezzoli L et al.
Journal of Cardiovascular Development and Disease, 2021
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO.
Sewani M et al.
American Journal of Medical Genetics. Part A, 2020
Case Report: Characterization of a Novel NONO Intronic Mutation in a Fetus With X-Linked Syndromic Mental Retardation-34.
Sun H et al.
Frontiers in Genetics, 2020
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