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Research 61–90 of 1000+
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Early onset androgenic alopecia as the male phenotypic equivalent of polycystic ovarian syndrome is associated in high oxidative stress
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- A guide to diagnosis and management of hypertrichosis
- Síndrome do nevo de Becker
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Cantú syndrome with coexisting familial pituitary adenoma
- Drug eruptions in dermatology
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Hirsutism and Hypertrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations