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Research 31–60 of 1000+
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Congenital hypotrichosis due to short anagen
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- 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.
- 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