Choanal Atresia and Craniosynostosis: Development and Disease.

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Choanal Atresia and Craniosynostosis: Development and Disease.

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http://www.wikidata.org/entity/Q47177604

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2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Choanal Atresia and Craniosynostosis: Development and Disease.

@en

Choanal Atresia and Craniosynostosis: Development and Disease.

@nl

type

Item

label

Choanal Atresia and Craniosynostosis: Development and Disease.

@en

Choanal Atresia and Craniosynostosis: Development and Disease.

@nl

prefLabel

Choanal Atresia and Craniosynostosis: Development and Disease.

@en

Choanal Atresia and Craniosynostosis: Development and Disease.

@nl

P1476

Choanal Atresia and Craniosynostosis: Development and Disease

@en

P2093

Ethylin Wang Jabs

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Joan T Richtsmeier

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Joseph M Bernstein

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Kate M Lesciotto

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P2860

Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Early development of the nose in human embryos: a stereomicroscopic and histologic analysis.

Choanal atresia and choanal stenosis.

Choanal atresia: current concepts and controversies.

Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia.

Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.

A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

Craniosynostosis syndromes: from genes to premature fusion of skull bones.

Midface anomalies in children.

P304

156-168

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P31

scholarly article

review article

P356

10.1097/PRS.0000000000003928

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P407

English

P433

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P478

141

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P50

Y Heuze

P577

2018-01-01T00:00:00Z

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P698

29280877

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P921

craniosynostosis

P932

5747311

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