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

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

Journal of medical genetics - 1 Aug 2002

Faivre L, Cormier-Daire V, Lapierre J M, Colleaux L, Jacquemont S, Geneviéve D, Saunier P, Munnich A, Turleau C, Romana S, Prieur M, De Blois M C, Vekemans M

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 Basic Helix-Loop-Helix Transcription Factors
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 6

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diagnosis, Differential

Share to Gene Deletion

Share to Helix-Loop-Helix Motifs

Share to Prader-Willi Syndrome

Share to Repressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 12161602
DOI: 10.1136/jmg.39.8.594
PMCID: PMC1735217

Genes

SIM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.PMID 12161602Read ↗

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

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

Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.Semantic proximity Read ↗

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

Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.Semantic proximity Read ↗

1p36 deletion syndrome associated with Prader-Willi-like phenotype.Semantic proximity Read ↗

A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype.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 ↗

Endocrine phenotype of 6q16.1–q21 deletion involving <i>SIM1</i> and Prader–Willi syndrome‐like featuresSemantic proximity Read ↗

A Case of Prader-Willi Syndrome With a Deletion Including MAGEL2 , NDN , and MKRN3 , but Excluding SNRPN and SNORD116.Semantic proximity Read ↗

Atypical 15q11.2-q13 Deletions and the Prader-Willi PhenotypeSemantic proximity Read ↗

A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.Semantic proximity Read ↗

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