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Research 511–540 of 1000+
- Alopecia in Cronkhite-Canada syndrome
- Dysfunction of keratinocyte adhesion
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- The Roles of EDA2R in Ageing and Disease
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Approach to Alopecia in Dogs in Clinical Practice
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Polarized microscopy in genetic hair disorders: case series
- 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
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Congenital Atrichia: A Case Report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Molecular Basis of Hereditary Hair Diseases
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Dermatological diseases from a genetic perspective
- Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Clouston’s syndrome: a rare case report
- The Naked (N) Mutation, Chromosome 15
- Index
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- Hair Loss in Children, Etiologies, and Treatment
- El teorema del 0,7 o el otro teorema de Pitágoras
- N02. Hair and Nails
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development