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- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Molecular Basis of Hereditary Hair Diseases
- Disorders of the Hair and Nails
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
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