Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC‐C loci
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M. Carella | L. Garavelli | L. Zelante | A. Superti-Furga | A. Cavazza | F. Forzano | M. R. Piemontese | F. Franchi | A. Wischmeijer | S. Rosato | G. Albertini | C. Gelmini | E. Albertini