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Research 91–120 of 1000+
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Keratosis follicularis spinulosa decalvans in a female
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Recently Identified Forms of Epidermolysis Bullosa
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Current Genetics in Hair Diseases
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Nonscarring hair loss disorders
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Substance P in keratosis follicularis spinulosa decalvans
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Werner′s syndrome
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- The Genetics of Human Skin Disease
- Hair shaft structures in EDAR induced ectodermal dysplasia