The t(8;13)(p11;q11–12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP

By Shipley J.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 637-642

Oxford University Press

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Disruption of a novel MFS transporter gene, DIRC2 , by a familial renal cell carcinoma-associated t(2;3)(q35;q21)

By Nickerson M.  

Human Molecular Genetics, Vol. 11, Iss. 6, 2002-03 ,pp. : 641-649

Oxford University Press

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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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Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitution

By Kuiper R.P.  

Human Molecular Genetics, Vol. 12, Iss. 14, 2003-07 ,pp. : 1661-1669

Oxford University Press

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A cis- regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E

By Maass Philipp G.   Wirth Jutta   Aydin Atakan   Rump Andreas   Stricker Sigmar   Tinschert Sigrid   Otero Miguel   Tsuchimochi Kaneyuki   Goldring Mary B.   Luft Friedrich C.   Bhring Sylvia  

Human Molecular Genetics, Vol. 19, Iss. 5, 2010-03 ,pp. : 848-860

Oxford University Press

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