Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint

By Kurahashi Hiroki   Shaikh Tamim H.   Emanuel Beverly S.  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2727-2732

Oxford University Press

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Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm

By Tong Maoqing   Kato Takema   Yamada Kouji   Inagaki Hidehito   Kogo Hiroshi   Ohye Tamae   Tsutsumi Makiko   Wang Jieru   Emanuel Beverly S.   Kurahashi Hiroki  

Human Molecular Genetics, Vol. 19, Iss. 13, 2010-07 ,pp. : 2630-2637

Oxford University Press

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Fine mapping of the constitutional translocation t(11;22)(q23;q11)

By Tapia-Páez Isabel   O'Brien Kevin P.   Kost-Alimova Maria   Sahlén Sigrid   Kedra Darek   Bruder Carl E. G.   Andersson Björn   Roe Bruce A.   Hu Ping   Imreh Stephan   Blennow Elisabeth   Dumanski Jan P.  

Human Genetics, Vol. 106, Iss. 5, 2000-05 ,pp. : 506-516

Springer Publishing Company

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Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)

By Kurahashi Hiroki  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1665-1670

Oxford University Press

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The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific Alu-mediated recombination

By Hill Alexander S.   Foot Nicola J.   Chaplin Tracy L.   Young Bryan D.  

Human Molecular Genetics, Vol. 9, Iss. 10, 2000-06 ,pp. : 1525-1532

Oxford University Press

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