WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype.
Bacino CA; Dhar SU; Brunetti-Pierri N; Lee B; Bonnen PE; American Journal Of Medical Genetics. Part A, 2012, vol. 158A, issue 11, p 2917, ISSN 15524833. ISBN 15524833.

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