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- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Disease causing homozygous variants in the human hairless gene
- Marie-unna hereditary hypotrichosis
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Congenital atrichia with papular lesions
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Atrichia with papular lesions
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Genetics of Structural Hair Disorders
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Biology and Genetics of Hair
- Congenital hair loss disorders: Rare, but not too rare
- Morphological Approach to Hair Disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Congenital atrichia and hypotrichosis