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Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasiaWNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndromeA mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail typeRapp-Hodgkin syndrome and the tail of p63Enhanced Edar signalling has pleiotropic effects on craniofacial and cutaneous glands.Complete and removable partial prosthesis for a child with hypohidrotic ectodermal dysplasiaClouston syndrome associated with eccrine syringofibroadenoma.Oral rehabilitation of a patient with ectodermal dysplasia: A multidisciplinary approach.Image Gallery: Periorbital and temporal dermal melanocytosis of hypohidrotic ectodermal dysplasia.Differential diagnosis of hair loss in children.Orofacial features of hypohidrotic ectodermal dysplasiaImplants in children with ectodermal dysplasia: a case report and literature review.Ectodermal Dysplasia: Management of Knife-Edged Irregular Ridge and Its Rehabilitation with Hybrid Implant ProsthesisEctodermal dysplasia with amastia: a case of one-step reconstruction.Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review.Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature.Connexin channels in congenital skin disorders.Human diseases associated with connexin mutations.Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong SyndromeHypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentationADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene.Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.Gene screening facilitates diagnosis of complicated symptoms: A case report.A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia.Dentomaxillofacial characteristics of ectodermal dysplasia.A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.Craniofacial growth and functional change in oligodontia with ectodermal dysplasia: a case report.2008 International Conference on Ectodermal Dysplasias Classification: conference report.Ectodermal Dysplasia: A Clinical Overview for the Dental Practitioner.Second International Conference on a classification of ectodermal dysplasias: Development of a multiaxis model
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Towards a new classification of ectodermal dysplasias.
@ast
Towards a new classification of ectodermal dysplasias.
@en
type
label
Towards a new classification of ectodermal dysplasias.
@ast
Towards a new classification of ectodermal dysplasias.
@en
prefLabel
Towards a new classification of ectodermal dysplasias.
@ast
Towards a new classification of ectodermal dysplasias.
@en
P2860
P1476
Towards a new classification of ectodermal dysplasias
@en
P2093
Lamartine J
P2860
P304
P356
10.1046/J.1365-2230.2003.01319.X
P577
2003-07-01T00:00:00Z