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Research 30 of 1000+
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Congenital hypotrichosis due to short anagen
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Congenital hypotrichosis in a French bulldog
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from South Dakota
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Congenital hypotrichosis - treatment with topical minoxidil and hair dye
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Familial congenital generalized hypertrichosis
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Congenital atrichia and hypotrichosis
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Hypotrichosis congenita of Marie Unna
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Hypertrichosis