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

MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34

22 Feb 2006

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 Congenital gastrointestinal and neural anomalies
Share to Congenital heart defects research
Share to Genetics and Neurodevelopmental Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16493448
DOI: 10.1038/sj.ejhg.5201577

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

MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34PMID 16493448Read ↗

[Genetic causes of mental retardation].Semantic proximity Read ↗

Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14.Semantic proximity Read ↗

Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?Semantic proximity Read ↗

Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.Semantic proximity Read ↗

Complex aetiology of an apparently Mendelian form of mental retardation.Semantic proximity Read ↗

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?Semantic proximity Read ↗

Hirschsprung's Disease: Genetic and Functional Associations of Down's and Waardenburg SyndromesSemantic proximity Read ↗

Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: alternative definition and further delineation of MOMO syndrome.Semantic proximity Read ↗

An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.Semantic proximity Read ↗

A Novel Mutation in the Endothelin B Receptor Gene in a Moroccan Family with Shah-Waardenburg SyndromeSemantic proximity Read ↗

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.Semantic proximity Read ↗

Mosaic Down's syndrome prevalence in a complete population studySemantic proximity Read ↗

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