Central nervous system malformations and deformations in FGFR2-related craniosynostosis. - Wikidata - wikimedia - TriplyDB

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

http://www.wikidata.org/entity/Q54482923

about

A Genetic-Pathophysiological Framework for Craniosynostosis Apert syndrome: temporal lobe abnormalities on fetal brain imaging.Infantile hydrocephalus: a review of epidemiology, classification and causes.Fibroblast Growth Factor Receptor-2 Contributes to the Basic Fibroblast Growth Factor-Induced Neuronal Differentiation in Canine Bone Marrow Stromal Cells via Phosphoinositide 3-Kinase/Akt Signaling Pathway The Morphogenesis of Cranial Sutures in Zebrafish.Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.Two Hundred Thirty-Six Children With Developmental Hydrocephalus: Causes and Clinical Consequences.Distinct selective forces and Neanderthal introgression shaped genetic diversity at genes involved in neurodevelopmental disorders.Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis.Shape and volume of craniofacial cavities in intentional skull deformations.Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges.Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes

P2860

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P2860

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

http://www.wikidata.org/entity/Q54482923

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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name

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@en

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@nl

type

label

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@en

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@nl

prefLabel

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@en

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@nl

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P1433

American Journal of Medical Genetics

P1476

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

@en

P2093

Anne-Lise Delezoide

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

Bettina Bessières

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Catherine Fallet-Bianco

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Jean M Hébert

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Valérie Bodiguel

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Wenfei Kang

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P2860

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

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

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

Dominant erbliche Akrocephalosyndaktylie

Hydrocephalus in craniosynostosis: a review.

The cerebral cortex malformation in thanatophoric dysplasia: neuropathology and pathogenesis.

Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.

The central nervous system in the Apert syndrome.

Apert's syndrome with central nervous system anomalies.

Expression of FGF receptors 1, 2, 3 in the embryonic and postnatal mouse brain compared with Pdgfralpha, Olig2 and Plp/dm20: implications for oligodendrocyte development.

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2797-2806

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scholarly article

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10.1002/AJMG.A.35598

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11

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158A

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Roman H Khonsari

Laurence Legeai-Mallet

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2012-09-17T00:00:00Z

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230871644

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craniosynostosis