Genetics and human malformations. - Test2 - elhamkhani - TriplyDB

Genetics and human malformations.

Genetics and human malformations.

http://www.wikidata.org/entity/Q37611550

about

A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts.Clinical correlate: Tooth Agenesis

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P2860

Genetics and human malformations.

http://www.wikidata.org/entity/Q37611550

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on September 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetics and human malformations.

@en

Genetics and human malformations.

@nl

type

label

Genetics and human malformations.

@en

Genetics and human malformations.

@nl

prefLabel

Genetics and human malformations.

@en

Genetics and human malformations.

@nl

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SCS.0B013E3181B2D3F3

P1433

Journal of Craniofacial Surgery

P1476

Genetics and human malformations

@en

P2093

Gabriele Mues

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

Hitesh Kapadia

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

Ying Wang

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

P2860

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

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

Epithelial-mesenchymal signalling regulating tooth morphogenesis.

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.

Significant correction of disease after postnatal administration of recombinant ectodysplasin A in canine X-linked ectodermal dysplasia.

Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.

Permanent correction of an inherited ectodermal dysplasia with recombinant EDA.

Pax genes and organogenesis: Pax9 meets tooth development.

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia.

P304

1652-1654

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scholarly article

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10.1097/SCS.0B013E3181B2D3F3

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P478

20 Suppl 2

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2009-09-01T00:00:00Z

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19816326

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2798143

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