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Research 30 of 1000+
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- [Wooly hair syndrome. Clinical and microscopic study].
- The inheritance of common baldness: Two B or not two B ?
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Monilethrix
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Pili Annulati: A case series and proposal for classification
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Woolly Hair in Two Siblings
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Inherited Disorders of the Hair
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Acquired Uncombable Hair
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Disorders of pigmentation in infants and children
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Monilethrix: A rare hereditary condition
- Monilethrix – Case report of a rare disease
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players