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

A 5-Mb microdeletion at 6q16.1-q16.3 with SIM gene deletion and obesity.

American journal of medical genetics. Part A - 15 Nov 2008

Wang Jia-Chi, Turner Lesley, Lomax Brenda, Eydoux Patrice

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Basic Helix-Loop-Helix Transcription Factors
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 6

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Developmental Disabilities

Share to Diagnosis, Differential

Share to In Situ Hybridization, Fluorescence

Share to Prader-Willi Syndrome

Source

Identifiers

PMID: 18925680
DOI: 10.1002/ajmg.a.32555

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

A 5-Mb microdeletion at 6q16.1-q16.3 with SIM gene deletion and obesity.PMID 18925680Read ↗

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.Semantic proximity Read ↗

Profound obesity associated with a balanced translocation that disrupts the SIM1 gene.Semantic proximity Read ↗

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.Semantic proximity Read ↗

A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.Semantic proximity Read ↗

Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.Semantic proximity Read ↗

A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis.Semantic proximity Read ↗

A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysisSemantic proximity Read ↗

Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delay.Semantic proximity Read ↗

190-kb duplication in 1p36.11 including PIGV and ARID1A genes in a girl with intellectual disability and hexadactyly.Semantic proximity Read ↗

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.Semantic proximity Read ↗

Studies of the SIM1 gene in relation to human obesity and obesity-related traits.Semantic proximity Read ↗

Analysis of the SIM1 contribution to polygenic obesity in the French population.Semantic proximity Read ↗

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