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

Sacral appendage in a child with an FGFR2 mutation: a report and review.

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

Shanske Alan L, Staffenberg David, Goodrich James T

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 Craniofacial Dysostosis
Share to Craniosynostoses
Share to FGFR2 gene
Share to Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Receptor, Fibroblast Growth Factor, Type 2

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 18629881
DOI: 10.1002/ajmg.a.32436

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sacral appendage in a child with an FGFR2 mutation: a report and review.PMID 18629881Read ↗

A mutation in FGFR2 in a child with Pfeiffer syndrome and a sacral appendage.Semantic proximity Read ↗

Sacral appendage associated with a mutation in FGFR2.Semantic proximity Read ↗

Kyphomelic dysplasia, phenotypic variability and presence of a caudal appendage.Semantic proximity Read ↗

A case report of mesenteric heterotopic ossification: Histopathologic and genetic findings.Semantic proximity Read ↗

Fibroblast growth factor receptors, developmental corruption and malignant diseaseSemantic proximity Read ↗

Review of genetic factors in intestinal malrotation.Semantic proximity Read ↗

Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review.Semantic proximity Read ↗

[Malignant bowel obstruction in peritoneal carcinosis from a serous ovarian carcinoma in a woman carrying high grade BRCA mutation: a case report].Semantic proximity Read ↗

Pathologic quiz case: multiple congenital birth defects in a full-term infant. Urorectal septum malformation sequence.Semantic proximity Read ↗

FGFR-associated craniosynostosis syndromes and gastrointestinal defects.Semantic proximity Read ↗

Management of Congenital Pouch Colon: Surgical Outcomes and Long-Term Follow-UpSemantic proximity Read ↗

Cutaneous appendage tumors: familial cylindromatosis and associated tumors update.Semantic proximity Read ↗

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