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Filters: Keyword is Ectodermal Dysplasia and Author is Dhar, Shweta U  [Clear All Filters]
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Bacino CA, Dhar SU, Brunetti-Pierri N, Lee B, Bonnen PE. WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. Am J Med Genet A. 2012 ;158A(11):2917-24.