A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions

By Yu Tao   Li Zhongyou   Jia Zhengping   Clapcote Steven J.   Liu Chunhong   Li Shaomin   Asrar Suhail   Pao Annie   Chen Rongqing   Fan Ni   Carattini-Rivera Sandra   Bechard Allison R.   Spring Shoshana   Henkelman R. Mark   Stoica George   Matsui Sei-Ichi   Nowak Norma J.   Roder John C.   Chen Chu   Bradley Allan   Yu Y. Eugene  

Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2780-2791

Oxford University Press

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The mouse Y chromosome interval necessary for spermatogonial proliferation is gene dense with syntenic homology to the human AZFa region

By Greenfield A.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1713-1724

Oxford University Press

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Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13–p16

By Cox D.W.  

Human Molecular Genetics, Vol. 8, Iss. 3, 1999-03 ,pp. : 501-507

Oxford University Press

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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

By Cruts Marc   Rademakers Rosa   van der Zee Julie   Dermaut Bart   de Pooter Tim   de Rijk Peter   Del-Favero Jurgen   van Broeckhoven Christine  

Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1753-1762

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A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3

By Sertié A. L.   Quimby M.   Moreira E. S.   Murray J.   Zatz M.   Antonarakis S. E.   Passos-Bueno M. R.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 843-847

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