hypotrichosis with juvenile macular dystrophy
SOX18 and the Hypotrichosis-Lymphedema-Telangiectasia Syndrome
Brief communication. Shorn (shn): a new mutation causing hypotrichosis in the Norway rat
Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome
Brief communication. The hypotrichosis-generating shorn (shn) mutation maps to distal chromosome 7 in the Norway rat
Arap3 is dysregulated in a mouse model of hypotrichosis–lymphedema–telangiectasia and regulates lymphatic vascular development
Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel maturation
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n. a condition in which less hair develops than normal.
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