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Research 31–60 of 1000+
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Inherited Disorders of the Hair
- Congenital Atrichia: A Case Report
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Biology and Genetics of Hair
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- New clinico‐genetic classification of trichothiodystrophy
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Genetic Hair Disorders: A Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Hair shaft disorders in children – An update
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- PA33 When bones speak through nails: insights from a paediatric case series
- Current Genetics in Hair Diseases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Salivary Gland Choristoma (Heterotopic Salivary Gland Tissue) on the Anterior Chest Wall of a Newborn
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Regulation of masculinization: androgen signalling for external genitalia development
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Acquired Uncombable Hair
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice