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Article

A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome.

American journal of medical genetics. Part A - 1 Oct 2017

Machado Renato A, Ferreira Shirlene B, Martins Luciane, Ribeiro Mariana M, Martelli Daniella R B, Coletta Ricardo D, Aguiar Marcos J B, Martelli-Júnior Hercílio

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Source

Identifiers

PMID: 28815901
DOI: 10.1002/ajmg.a.38389

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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