Chimeric Negative Regulation ofp14ARFandTBX1by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency-Reference-Cited by-同舟云学术

Chimeric Negative Regulation ofp14ARFandTBX1by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency

Published:2013-06-03 Issue:9 Volume:34 Page:1250-1259
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Tan Xiaohui¹,Anzick Sarah L.²,Khan Sikandar G.¹,Ueda Takahiro¹,Stone Gary²,DiGiovanna John J.¹,Tamura Deborah¹,Wattendorf Daniel³,Busch David⁴,Brewer Carmen C.⁵,Zalewski Christopher⁵,Butman John A.⁶,Griffith Andrew J.⁵,Meltzer Paul S.²,Kraemer Kenneth H.¹

Affiliation:

1. DNA Repair Section, Dermatology Branch, Center for Cancer Research; National Cancer Institute; Bethesda Maryland

2. Genetics Branch, Center for Cancer Research; National Cancer Institute; Bethesda Maryland

3. Office of the Air Force Surgeon General; Washington DC

4. Armed Forces Institute of Pathology; Washington DC

5. Otolaryngology Branch; National Institute of Deafness and Communication Disorders; Bethesda Maryland

6. Radiology Branch, Clinical Center; National Institutes of Health; Bethesda Maryland

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22354/fullpdf

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5. Evolutionary forces shape the human RFPL1,2,3 genes toward a role in neocortex development;Bonnefont;Am J Hum Genet,2008

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