Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2)
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/3/6/937/1608329/3-6-937.pdf
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney;Human Molecular Genetics;2004-07-14
2. Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2;Journal of Medical Genetics;2004-07-01
3. Coexistence of Autosomal Dominant Polycystic Kidney Disease and Neurofibromatosis: Report of a Family;American Journal of Nephrology;2002
4. Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation;Human Genetics;2001-08-01
5. Neurofibromatosen;Molekularmedizinische Grundlagen von hereditären Tumorerkrankungen;2001
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