Biblio

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Filters: Author is Kwan,Kenneth Y. [Clear All Filters]

2010

[1802] Bilguvar, K., Ozturk A K., Louvi A., Kwan K. Y., Choi M., Tatli B., et al. (2010). Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. advance online publication,