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

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat‐Wilson syndrome

7 Oct 2002

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 Gastrointestinal disorders and treatments
Share to Intestinal Malrotation and Obstruction Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12522797
DOI: 10.1002/ajmg.a.10855

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

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat‐Wilson syndromePMID 12522797Read ↗

Mowat-Wilson syndrome.Semantic proximity Read ↗

A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.Semantic proximity Read ↗

ZFHX1B mutations in patients with Mowat-Wilson syndrome.Semantic proximity Read ↗

"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.Semantic proximity Read ↗

Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.Semantic proximity Read ↗

Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1Semantic proximity Read ↗

Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity.Semantic proximity Read ↗

Mowat-Wilson syndrome.Semantic proximity Read ↗

A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.Semantic proximity Read ↗

Mowat--Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p.T791fsX816).Semantic proximity Read ↗

Clinical characteristics and novel ZEB2 gene mutation analysis of three Chinese patients with Mowat-Wilson syndromeSemantic proximity Read ↗

Clinical and mutational spectrum of Mowat-Wilson syndrome.Semantic proximity Read ↗

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