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5. Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome. Saleem MD Pediatr Dermatol; 2019 Jan; 36(1):72-84. PubMed ID: 30561083 [TBL] [Abstract][Full Text] [Related]
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8. Piebaldism. More V; Sharma R; Thomas V Indian Pediatr; 2011 Aug; 48(8):665-6. PubMed ID: 21918288 [No Abstract] [Full Text] [Related]
9. [Piebaldisme: a rare genodermatosis]. Debbarh FZ; Mernissi FZ Pan Afr Med J; 2017; 27():221. PubMed ID: 28979623 [TBL] [Abstract][Full Text] [Related]
10. A novel KIT missense mutation in one Chinese family with piebaldism. Yin XY; Ren YQ; Yang S; Xu SX; Zhou FS; Du WH; Lin D; Wang PG; Zhang SM; Zhang XJ Arch Dermatol Res; 2009 Jun; 301(5):387-9. PubMed ID: 19430803 [TBL] [Abstract][Full Text] [Related]
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12. Piebaldism--a case report. Hwang SM; Ahn SK; Lee WS; Yoo MS; Choi EH J Korean Med Sci; 1996 Jun; 11(3):285-8. PubMed ID: 8843015 [TBL] [Abstract][Full Text] [Related]
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15. Piebaldism in a 3-month-old infant--case report. Milankov O; Savić R; Radulović A Med Pregl; 2014; 67(3-4):109-10. PubMed ID: 24961053 [TBL] [Abstract][Full Text] [Related]
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18. Striking contiguous depigmentation across the lower limbs in piebaldism and its implications for understanding melanocytic migration and development. Funkhouser CH; Kinsler VA; Frieden IJ Pediatr Dermatol; 2019 Jul; 36(4):511-513. PubMed ID: 30983016 [TBL] [Abstract][Full Text] [Related]
19. A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype. Chong KL; Common JE; Lane EB; Goh BK J Dermatol Sci; 2010 Sep; 59(3):206-9. PubMed ID: 20688482 [No Abstract] [Full Text] [Related]
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