Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

By Ried Karin  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1651-1663

Oxford University Press

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Common chromosomal fragile site FRA16D mutation in cancer cells

By Finnis Merran  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1341-1349

Oxford University Press

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The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers

By Blumrich Anne   Zapatka Marc   Brueckner Lena M.   Zheglo Diana   Schwab Manfred   Savelyeva Larissa  

Human Molecular Genetics, Vol. 20, Iss. 8, 2011-04 ,pp. : 1488-1501

Oxford University Press

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Impaired replication dynamics at the FRA3B common fragile site

By Palakodeti Aparna   Lucas Isabelle   Jiang Yanwen   Young David J.   Fernald Anthony A.   Karrison Theodore   Le Beau Michelle M.  

Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 99-110

Oxford University Press

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FRA3B Extends Over a Broad Region and Contains a Spontaneous HPV16 Integration Site: Direct Evidence for the Coincidence of Viral Integration Sites and Fragile Sites

By Wilke Charles M.   Hall Bryan K.   Hoge Ann   Paradee William   Smith David I.   Glover Thomas W.  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 187-195

Oxford University Press

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