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Research 961–990 of 1000+
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia and hypotrichosis
- Clinical Case Notes. Propecia-associated bilateral cataract
- Hair loss among a group of Egyptian children
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- 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
- Expression ofWise in chick embryos
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- What Syndrome Is This?
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Using High-Throughput Immunoblotting to Identify Proteins Involved in the Differentiation of ES Cells along the Hair Follicle Lineage in Vitro
- Connexin mutations in human disease
- Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia
- 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
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- 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