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Article

[Prenatal diagnosis of Apert syndrome caused by de novo mutation in FGFR2 gene].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Mar 2014

Pi G, Zúñiga A, Cervera J, Ortiz M

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Topics

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Share to Acrocephalosyndactylia
Share to Fatal Outcome
Share to FGFR2 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptor, Fibroblast Growth Factor, Type 2

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 24286882
DOI: 10.1016/j.anpedi.2013.09.013

Genes

FGFR2

Provenance

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

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[Prenatal diagnosis of Apert syndrome caused by de novo mutation in FGFR2 gene].PMID 24286882Read ↗

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[FGFR2 gene mutation in a Chinese patient with Apert syndrome].Semantic proximity Read ↗

[Apert syndrome or acrocephalosyndactilia type I].Semantic proximity Read ↗

Identification of a Novel FGFR2 Gene Mutation (c.514_515delinsCT, p.Ala172Leu) in a Chinese Neonate With Apert Syndrome: A Case Report.Semantic proximity Read ↗

Apert syndrome: A case report of prenatal ultrasound, postmortem cranial CT, and molecular genetic analysis.Semantic proximity Read ↗

p.Ser252Trp and p.Pro253Arg mutations in FGFR2 gene causing Apert syndrome: the first clinical and molecular report of Indonesian patients.Semantic proximity Read ↗

[Apert syndrome: clinico-epidemiological analysis of a series of consecutive cases in Spain].Semantic proximity Read ↗

Prenatal diagnosis and management of Apert syndrome in a low-middle income country: Case reportSemantic proximity Read ↗

Mutations in the FGFR2 gene in Mexican patients with Apert syndrome.Semantic proximity Read ↗

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