Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22-Reference-Cited by-同舟云学术

Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22

Author:

Byers Heather M.¹²,Adam Margaret P.²³,LaCroix Amy³,Leary Sarah E. S.⁴,Cole Bonnie⁵,Dobyns William B.²³⁶⁷,Mefford Heather C.²³

Affiliation:

1. Division of Medical Genetics; Department of Medicine; University of Washington; Seattle Washington

2. Division of Genetic Medicine; Seattle Children's Hospital; Seattle Washington

3. Division of Genetic Medicine; Department of Pediatrics; University of Washington; Seattle Washington

4. Division of Oncology; Seattle Children's Hospital; Seattle Washington

5. Department of Laboratories; Seattle Children's Hospital; Seattle Washington

6. Center for Integrative Brain Research; Seattle Children's Research Institute; Seattle Washington

7. Department of Neurology; University of Washington; Seattle Washington

Funder

NIH

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference22 articles.

1. Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors;Biegel;Cancer Res,1999

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3. Ring Chromosome 22;Human Ring Chromosomes;2024