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- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Genetics of Structural Hair Disorders
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Diffuse hypotrichosis from early childhood
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Genetics of Alopecia
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Brief study of hypertrichosis
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Genetic Hair Disorders: A Review
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hypotrichosis with juvenile macular dystrophy
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Polarized microscopy in genetic hair disorders: case series
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the <i>LIPH</i> gene at c.742C > A and c.614A > G: The first Japanese case
- Hypotrichosis and Alopecia
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Dermatological diseases from a genetic perspective
- Autosomal recessive hereditary hypotrichosis simplex: A case report