Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Identification of a NONO gene variant in a child with congenital heart disease and global developmental delay].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Jun 2023

Lei Yuqing, Peng Xiaoyan, Wang Xinrui, Cao Hua

Abstract excerpt

OBJECTIVE: To explore the genetic basis for a child with congenital heart disease (CHD) and global developmental delay (GDD). METHODS: A child who was hospitalized at the Department of Cardiac Surgery of Fujian Children's Hospital on April 27, 2022 was selected as the study subject. Clinical data of the child was collected. Umbilical cord blood sample of the child and peripheral blood samples of his parents were...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Computational Biology
Share to Developmental Disabilities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-Binding Proteins

Share to Genetic Counseling

Share to Genomics

Share to Heart Defects, Congenital

Share to Parents

Share to RNA-Binding Proteins

Source

Identifiers

PMID: 37212004
DOI: 10.3760/cma.j.cn511374-20220730-00508

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Identification of a NONO gene variant in a child with congenital heart disease and global developmental delay].PMID 37212004Read ↗

[Clinical and genetic analysis of a Chinese pedigree affected with MRXS34 syndrome due to variant of NONO gene].Semantic proximity Read ↗

Navigating the non-coding genome in heart development and Congenital Heart DiseaseSemantic proximity Read ↗

[Clinical and genetic analysis of a child with MRXS34 syndrome due to variant of NONO gene].Semantic proximity Read ↗

RCAN family member 3 deficiency contributes to noncompaction of the ventricular myocardiumSemantic proximity Read ↗

[Analysis of NSD1 gene variant in a child with autism spectrum disorder in conjunct with congenital heart disease].Semantic proximity Read ↗

[Clinical and genetic analysis of Noonan syndrome in 20 children].Semantic proximity Read ↗

[Clinical phenotype and genetic analysis of a fetus with Cardiac valvular dysplasia type 1].Semantic proximity Read ↗

[Analysis of a child with You-Hoover-Fong syndrome due to compound heterozygous variants of the TELO2 gene and a literature review].Semantic proximity Read ↗

Genetic Architecture of CHD in NICU patients – UMC Ljubljana ExperienceSemantic proximity Read ↗

A Novel Mutation of NONO-Associated X-linked Syndromic Intellectual Developmental Disorder-34 in a FetusSemantic proximity Read ↗

[Analysis of a child with Osteo-oto-hepato-enteric syndrome and a literature review].Semantic proximity Read ↗

[Clinical and genetic analysis of a child with Culler-Jones syndrome due to variant of GLI2 gene].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.