Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors
Open Access
- 1 August 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (2) , 295-303
- https://doi.org/10.1086/514854
Abstract
No abstract availableKeywords
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