Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and ST14[original query] |
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A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome. Orphanet journal of rare diseases 2017 12 12 (1): 176. Youssefian Leila, Touati Andrew, Saeidian Amir Hossein, Zargari Omid, Zeinali Sirous, Vahidnezhad Hassan, Uitto Jou |
Clinical and molecular characteristics of autosomal recessive congenital ichthyosis in Thailand. Pediatric dermatology 2022 Oct . Supsrisunjai Chavalit, Bunnag Thareena, Chaowalit Prapaipit, Boonpuen Niorn, Kootiratrakarn Tanawatt, Wessagowit Vesar |
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- Page last updated:May 06, 2024
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