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- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- The amazing miniorgan: Hair follicle
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Ichthyosis with confetti: clinics, molecular genetics and management
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Ectodermal Dysplasia: Variable Expressions
- Polarized microscopy in genetic hair disorders: case series
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Trichoscopy in Hair Shaft Disorders
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathology and molecular genetics
- Congenital atrichia and hypotrichosis
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
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- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Inherited Disorders of the Hair
- Hypotrichosis congenita of Marie Unna
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Hair: more than just an appendage
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- A New Case of Isolated Trichothiodystrophy