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

Phenotype of five patients with Greig syndrome and microdeletion of 7p13.

American journal of medical genetics - 15 Aug 2001

Kroisel P M, Petek E, Wagner K

Abstract excerpt

Here we describe five patients with Greig cephalopolysyndactyly syndrome (GCPS), including one pair of monozygotic twin boys with a de novo microdeletion involving the chromosomal band 7p13, where various clinical manifestations, in addition to GCPS, were recognized. Besides the twin pair, all pa...

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 Chromosome Deletion
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Craniofacial Abnormalities

Share to In Situ Hybridization, Fluorescence

Share to Syndactyly

Share to Syndrome

Share to Twins, Monozygotic

Source

Identifiers

PMID: 11484201
DOI: 10.1002/ajmg.1443

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11484201-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotype of five patients with Greig syndrome and microdeletion of 7p13.PMID 11484201Read ↗

The Greig cephalopolysyndactyly syndromeSemantic proximity Read ↗

[7p14.1 microdeletion and Greig cephalopolysyndactyly syndrome].Semantic proximity Read ↗

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.Semantic proximity Read ↗

The clinical atlas of Greig cephalopolysyndactyly syndromeSemantic proximity Read ↗

Two Indian families with Greig cephalopolysyndactyly with non-syndromic phenotype.Semantic proximity Read ↗

Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.Semantic proximity Read ↗

Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.Semantic proximity Read ↗

[Greig cephalopolysyndactyly syndrome].Semantic proximity Read ↗

Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.Semantic proximity Read ↗

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations.Semantic proximity Read ↗

Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotypeSemantic proximity Read ↗

TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION.Semantic proximity Read ↗

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