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Article

Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation.

Indian journal of pediatrics - 1 Jun 2020

Goyal Manisha, Gupta Ashok, Kapoor Seema, Bhandari Anu

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 31879841
DOI: 10.1007/s12098-019-03140-x

Genes

FGFR2

Provenance

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Related research

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Research trail→

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Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation.PMID 31879841Read ↗

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

Apert syndrome.Semantic proximity Read ↗

Apert syndrome with partial preaxial polydactyly.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 ↗

Atypical presentation of a newborn with Apert syndrome.Semantic proximity Read ↗

Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation.Semantic proximity Read ↗

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

Apert syndrome with omphalocele: a case report.Semantic proximity Read ↗

Prenatal Diagnosis of Apert Syndrome due to A De novo FGFR2 Mutation at the Second Trimester: a case reportSemantic proximity Read ↗

Prenatal diagnosis of Apert syndrome caused by a de novo FGFR2 mutation in the second trimester: a case report.Semantic proximity Read ↗

Genetic overview of postaxial polydactyly: Updated classificationSemantic proximity Read ↗

Understanding the molecular basis of Apert syndrome.Semantic proximity Read ↗

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