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Publications by Mary Fete
Ectodermal Dysplasias: Classification and Organization by Phenotype, Genotype and Molecular Pathway
American Journal of Medical Genetics, Part A
Genetics
Characterization of X-Linked Hypohidrotic Ectodermal Dysplasia (XL-HED) Hair and Sweat Gland Phenotypes Using Phototrichogram Analysis and Live Confocal Imaging
American Journal of Medical Genetics, Part A
Genetics
Related publications
Ectodermal Dysplasias Revisited
Acta geneticae medicae et gemellologiae
DLX Genes, P63, and Ectodermal Dysplasias
Birth Defects Research Part C - Embryo Today: Reviews
Medicine
Embryology
Developmental Biology
Genotype-Phenotype Correlation of PLOD2 Skeletal Dysplasias Using Structural Information
Journal of Bone and Mineral Research
Endocrinology
Orthopedics
Sports Medicine
Metabolism
Diabetes
Pathogenic EDA Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype–Phenotype: A Correlation Analysis
Frontiers in Genetics
Genetics
Molecular Medicine
Differential Altered Stability and Transcriptional Activity of Np63 Mutants in Distinct Ectodermal Dysplasias
Journal of Cell Science
Cell Biology
Deep Phenotyping: Deep Learning for Temporal Phenotype/Genotype Classification
Plant Methods
Biotechnology
Plant Science
Genetics
Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14
American Journal of Human Genetics
Genetics
Homeobox Gene Dlx3 Is Regulated by P63 During Ectoderm Development: Relevance in the Pathogenesis of Ectodermal Dysplasias
Development (Cambridge)
Developmental Biology
Molecular Biology
Genotype–phenotype Correlations in THAP1 Dystonia: Molecular Foundations and Description of New Cases
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
