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Research 361–390 of 1000+
- 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
- Inherited Disorders of the Hair
- 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
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Alopecia in a 19-Month-Old Boy
- Acquired uncombable hair
- [Wooly hair syndrome. Clinical and microscopic study].
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Ugreelig hår
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- A Newborn With Hair Loss
- Familial congenital generalized hypertrichosis
- Woolly Antics between the Sheaths
- Reply
- Spatiotemporal secondary hair follicle development in the Lanyu pig (Sus scrofa taivanus): a novel pelage hair follicle model
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report