Ectodermal Dysplasias: A Clinical and Molecular Review
Author:
Publisher
Elsevier BV
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Reference171 articles.
1. Langman embriología médica: con orientación clínica;Sadler,2008
2. Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanism;Priolo;Am J Med Genet A,2009
3. Mendelian Inheritance in Man: A catalog of Human Genes and Genetic Disorders;McKusick,1998
4. Rationale and background as basis for a new classification of the ectodermal dysplasias;Itin;Am J Med Genet A,2009
5. Only four genes (EDA1, EDAR, EDARADD and WNTA10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases;Cluzeau;Hum Mutat,2011
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5. Phenotypic Features and Salivary Parameters in Patients with Ectodermal Dysplasia: Report of Three Cases;Case Reports in Dentistry;2018
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