Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
about
Axl promotes the proliferation, invasion and migration of Wilms' tumor and can be used as a prognostic factor.The roles of microRNAs in Wilms' tumors.K-Ras, H-Ras, N-Ras and B-Raf mutation and expression analysis in Wilms tumors: association with tumor growth.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.Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies
P2860
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
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2012年學術文章
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name
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@en
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@nl
type
label
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@en
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@nl
prefLabel
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@en
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@nl
P2093
P2860
P50
P356
P1476
Wilms' tumor in patients with ...... for PTCH1 in nephroblastomas.
@en
P2093
Albert David
Annaig Briand
Bertrand Isidor
Caroline Kannengiesser
Delfine Lafon
Dominique Martin-Coignard
Elodie Lacaze
Ghislaine Plessis
Maria Piccione
Nicolas Sévenet
P2860
P2888
P304
P356
10.1038/EJHG.2012.252
P577
2012-11-21T00:00:00Z