Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

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Gene/environment interactions in craniosynostosis: A brief review.Crouzon syndrome: Genetic and intervention review Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit

P2860

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P2860

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

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http://www.wikidata.org/entity/Q39993560

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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2016年學術文章

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name

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

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Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@nl

type

Item

label

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@en

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@nl

prefLabel

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@en

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@nl

P1476

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

@en

P2093

Amy Kreithen

http://www.w3.org/2001/XMLSchema#string

Gregory M Cooper

http://www.w3.org/2001/XMLSchema#string

James J Cray

http://www.w3.org/2001/XMLSchema#string

James R Gilbert

http://www.w3.org/2001/XMLSchema#string

Joseph E Losee

http://www.w3.org/2001/XMLSchema#string

Mark P Mooney

http://www.w3.org/2001/XMLSchema#string

Mary L Marazita

http://www.w3.org/2001/XMLSchema#string

Michael I Siegel

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P2860

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

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

Comparison of craniofacial phenotype in craniosynostotic rabbits treated with anti-Tgf-beta2 at suturectomy site.

Genetic study of scaphocephaly.

Craniosynostosis: genes and mechanisms.

Cranial sutures: a brief review.

Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of Origin

FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report.

A TWIST in the fate of human osteoblasts identifies signaling molecules involved in skull development.

Sutural biology and the correlates of craniosynostosis.

P304

94-99

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scholarly article

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10.1597/15-226

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English

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2016-02-16T00:00:00Z

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P698

26882022

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Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

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P2860

P2860

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.

description

name

type

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prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698