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Publications by Newton Freire-Maia
Ectodermal Dysplasias Revisited
Acta geneticae medicae et gemellologiae
Related publications
DLX Genes, P63, and Ectodermal Dysplasias
Birth Defects Research Part C - Embryo Today: Reviews
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Ectodermal Dysplasias: Classification and Organization by Phenotype, Genotype and Molecular Pathway
American Journal of Medical Genetics, Part A
Genetics
Differential Altered Stability and Transcriptional Activity of Np63 Mutants in Distinct Ectodermal Dysplasias
Journal of Cell Science
Cell Biology
A Human Stem Cell-Based System to Study the Role of TP63 Mutations in Ectodermal Dysplasias
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
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Homeobox Gene Dlx3 Is Regulated by P63 During Ectoderm Development: Relevance in the Pathogenesis of Ectodermal Dysplasias
Development (Cambridge)
Developmental Biology
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From the Transcription of Genes Involved in Ectodermal Dysplasias to the Understanding of Associated Dental Anomalies
Molecular Syndromology
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Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14
American Journal of Human Genetics
Genetics
Skeletal Dysplasias
Clinics in Perinatology
Gynecology
Child Health
Pediatrics
Perinatology
Obstetrics
Hypohidrotic Ectodermal Dysplasia
