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Research 181–210 of 1000+
- Atrichia With Papular Lesions
- Familial Nonmembranous Aplasia Cutis of the Scalp
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Monilethrix: A rare hereditary condition
- Short anagen hair syndrome
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- A new type of pachyonychia congenita.
- 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
- 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.
- 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
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2