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
Essential role of NONO-HOXA1-Wnt axis in cardiomyocyte differentiation.
Feng Z et al.
Nature Communications, 2026
Chromatin Meets Condensates: Emerging Interplays Linking Nuclear Paraspeckles to Gene Activation.
Tu CH et al.
Epigenetics Reports, 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
Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood.
French CE et al.
Hgg Advances, 2022
35586607 (PubMed )
Supplement: mmc2.xlsx › Sheet1
Select a paper to view details