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

[Genetic analysis of a child with Malan syndrome].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Nov 2024

Wang Baosong, Zhang Xuexi, Li Yunjia, Liu Tao, Li Lin, Meng Qin

Abstract excerpt

OBJECTIVE: To explore the genetic basis of a child with mental retardation and developmental delay. METHODS: A child who had attended the genetic clinic of Linyi People's Hospital from October 2023 to April 2024 was selected as the study subject. Intelligence and development were assessed with simplified Peabody scale. Electroencephalogram and imaging data were collected. Peripheral blood samples of the child and...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Developmental Disabilities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Intellectual Disability

Share to Mutation

Share to NFI Transcription Factors

Share to Phenotype

Share to Whole Genome Sequencing

Source

Identifiers

PMID: 39528283
DOI: 10.3760/cma.j.cn511374-20240621-00347

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Genetic analysis of a child with Malan syndrome].PMID 39528283Read ↗

[Clinical and genetic analysis of a child with X-linked intellectual developmental disorder due to a novel variant of NEXMIF gene].Semantic proximity Read ↗

[Clinical and genetic analysis of a child with X-linked mental retardation due to variant of SLC9A7 gene].Semantic proximity Read ↗

[Clinical and genetic analysis of a child with West syndrome due to a de novo variant of NEXMIF gene].Semantic proximity Read ↗

[Analysis of a child with neurodevelopmental disorders due to variant of HNRNPU gene and a literature review].Semantic proximity Read ↗

[Genetic analysis of a child with Dias-Logan syndrome due to variant of BCL11A gene].Semantic proximity Read ↗

[Analysis of a child with developmental disorder and epilepsy due to a homozygous variant of SLC25A12 gene].Semantic proximity Read ↗

[Analysis of genetic variants in a child with Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism without seizures].Semantic proximity Read ↗

[Clinical characteristics and genetic analysis of a child with Dyggve-Melchior-Clausen syndrome due to variant of DYM gene].Semantic proximity Read ↗

[Clinical and genetic analysis of a child with Mental retardation autosomal dominant 51].Semantic proximity Read ↗

[Analysis of a child with X-linked intellectual disability due to a maternal de novo splicing variant of the PAK3 gene].Semantic proximity Read ↗

The genetic architecture of monogenic neurodevelopmental disorders in Pakistan: a systematic review, 2006–2024Semantic proximity Read ↗

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

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