Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors-Reference-Cited by-同舟云学术

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Published:2009-10-25 Issue:11 Volume:41 Page:1247-1252
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Goriely Anne,Hansen Ruth M S,Taylor Indira B,Olesen Inge A,Jacobsen Grete Krag,McGowan Simon J,Pfeifer Susanne P,McVean Gilean A T,Meyts Ewa Rajpert-De,Wilkie Andrew O M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.470.pdf

Reference60 articles.

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4. Eble, J.N. Spermatocytic seminoma. Hum. Pathol. 25, 1035–1042 (1994).

5. Rajpert-De Meyts, E. et al. The immunohistochemical expression pattern of Chk2, p53, p19INK4d, MAGE-A4 and other selected antigens provides new evidence for the premeiotic origin of spermatocytic seminoma. Histopathology 42, 217–226 (2003).

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