A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
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Tooth agenesis and orofacial clefting: genetic brothers in arms?Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth AgenesisDNA methylation is critical for tooth agenesis: implications for sporadic non-syndromic anodontia and hypodontia.The Gene Network Underlying Hypodontia.Dental Age and Tooth Development in Orthodontic Patients with Agenesis of Permanent Teeth.Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.Prevalence and Characteristics of Congenitally Missing Permanent Teeth among Orthodontic Patients in Southern Croatia.
P2860
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P2860
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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name
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
@en
type
label
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
@en
prefLabel
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
@en
P2093
P1476
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family
@en
P2093
Ebtesam M Abdalla
Karin Dwidar
Suzan R Ismail
P304
P356
10.1016/J.ARCHORALBIO.2014.04.004
P577
2014-04-19T00:00:00Z