2008 International Conference on Ectodermal Dysplasias Classification: Conference report
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32882/fullpdf
Reference19 articles.
1. P63 gene mutations and human developmental syndromes;Brunner;Am J Med Genet,2002
2. Significant correction of disease after postnatal administration of recombinant ectodysplasin A in canine X-linked ectodermal dysplasia;Casal;Am J Hum Genet,2007
3. Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene;Clements;J Dermatol Sci,2007
4. Ectodermal dysplasias;Freire-Maia;Hum Hered,1971
5. Ectodermal dysplasias revisited;Freire-Maia;Acta Genet Med Gemellol,1977
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1. A digital workflow for tooth-supported complete overdentures with a composite resin injection technique to manage the treatment of a child with ectodermal dysplasia;The Journal of Prosthetic Dentistry;2024-01
2. Hypohidrotic ectodermal dysplasia: A case report with review and latest updates;Journal of Oral and Maxillofacial Pathology;2022
3. First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?;Italian Journal of Pediatrics;2021-06-02
4. A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families;The Journal of Gene Medicine;2019-08-05
5. Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway;American Journal of Medical Genetics Part A;2019-01-31
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