Search
for
Sort by
Research 61–90 of 1000+
- Short anagen hair syndrome
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- A new type of pachyonychia congenita.
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Eruptive Vellus Hair Cyst
- Masquerading of trichotillomania in a family with monilethrix
- Monilethrix in three generations
- 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
- Acquired Uncombable Hair
- Alopezien und Hypotrichosen im Kindesalter
- Spangled hair in siblings
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Monilethrix
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Marie-unna hereditary hypotrichosis
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Disorders of pigmentation in infants and children
- Alopecia in a 19-Month-Old Boy
- 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.
- Acquired uncombable hair
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis