Pfeiffer syndrome: clinical and genetic findings in five Brazilian families. - Test2 - elhamkhani - TriplyDB

Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

http://www.wikidata.org/entity/Q35059805

about

Understanding craniosynostosis as a growth disorder A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

http://www.wikidata.org/entity/Q35059805

description

2015 nî lūn-bûn

@nan

2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2015年の論文

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2015年論文

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2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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type

label

Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

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Medicina Oral, Patologia Oral y Cirugia Bucal

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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.

@en

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Hercílio-Martelli Júnior

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Letícia-Lima Leão

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Marcos-José Burle-Aguiar

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Renato-Assis Machado

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Ricardo-Della Coletta

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Sibele-Nascimento de Aquino

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P2860

Pfeiffer syndrome

Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

DOMINANT HEREDITARY ACROCEPHALOSYNDACTYLIA

Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis

Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome

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e52-8

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scholarly article

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10.4317/MEDORAL.20032

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1

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