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Research 91–120 of 1000+
- The fundamentals of WNT10A
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Disorders of the Hair and Scalp in Children
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Analogs of human genetic skin disease in domesticated animals
- 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
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- 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
- 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
- Dermatological diseases from a genetic perspective
- 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
- Hair Loss in Children, Etiologies, and Treatment
- El teorema del 0,7 o el otro teorema de Pitágoras
- N02. Hair and Nails
- Current Genetics in Hair Diseases