Associated Papers
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
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
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Roessler F et al.
American Journal of Medical Genetics. Part A, 2023
Biventricular non-compaction cardiomyopathy and tricuspid hypoplasia in a novel non-POU domain-containing octamer-binding gene variant.
Safi S et al.
Cardiology in the Young, 2022
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
Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndrome.
Carlston CM et al.
American Journal of Medical Genetics. Part A, 2019
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