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Research 451–480 of 1000+
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Congenital atrichia with papular lesions
- Eruptive Vellus Hair Cyst
- Siberian cats help in solving part of the mystery surrounding golden cats
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Monilethrix
- Masquerading of trichotillomania in a family with monilethrix
- Monilethrix in three generations
- Acquired Uncombable Hair
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Alopezien und Hypotrichosen im Kindesalter
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Spangled hair in siblings
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Congenital atrichia with papular lesions
- Marie-unna hereditary hypotrichosis
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Monilethrix
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Disorders of pigmentation in infants and children