Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1 (Q40761872)
scientific article published on December 15, 2001
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(P31) (Q13442814)
(P50) (Q52116879)
(Q39802515)
(P304) 2989-3000
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(P577) Saturday, December 1, 2001
Saturday, December 15, 2001
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(P953) https://academic.oup.com/hmg/article-pdf/10/26/2989/9813605/102989.pdf
http://academic.oup.com/hmg/article-pdf/10/26/2989/9813605/102989.pdf
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(P1476) "Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1" (language: en)
(P2093) R. Weksberg
J. Nishikawa
O. Caluseriu
Y. L. Fei
C. Shuman
C. Wei
L. Steele
J. Cameron
I. Ambus
M. Li
P. N. Ray
P. Sadowski
other details
description scientific article published on December 15, 2001

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