Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement

By Rodríguez-Perales Sandra   Meléndez Bárbara   Gribble Susan M.   Valle Laura   Carter Nigel P.   Santamaría Iñigo   Conde Lucia   Urioste Miguel   Benítez Javier   Cigudosa Juan C.  

Human Molecular Genetics, Vol. 13, Iss. 9, 2004-05 ,pp. : 983-990

Oxford University Press

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A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)

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Human Molecular Genetics, Vol. 12, Iss. 21, 2003-11 ,pp. : 2817-2825

Oxford University Press

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Understanding Mesenchymal Cancer: The Liposarcoma-Associated t(12;16) (q13;;p11) Chromosomal Translocation as a Model

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Current Genomics, Vol. 3, Iss. 4, 2002-08 ,pp. : 237-244

Bentham Science Publishers

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Molecular Genetic and Phenotypic Analysis Reveals Differences between TSC1 and TSC2 Associated Familial and Sporadic Tuberous Sclerosis

By Jones Alistair C.   Daniells Claire E.   Snell Russell G.   Tachataki Maria   Idziaszczyk Shelley A.   Krawczak Michael   Sampson Julian R.   Cheadle Jeremy P.  

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A Novel Familial BBS12 Mutation Associated with a Mild Phenotype: Implications for Clinical and Molecular Diagnostic Strategies

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Karger

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