Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes

By Shimizu N.  

Human Molecular Genetics, Vol. 12, Iss. 15, 2003-08 ,pp. : 1823-1837

Oxford University Press

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

By Shaikh Tamim H.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 489-501

Oxford University Press

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Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice

By Suzuki Go   Harper Kathryn M.   Hiramoto Takeshi   Funke Birgit   Lee MoonSook   Kang Gina   Buell Mahalah   Geyer Mark A.   Kucherlapati Raju   Morrow Bernice   Mnnist Pekka T.   Agatsuma Soh   Hiroi Noboru  

Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3914-3925

Oxford University Press

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A Mouse Splice-Site Mutant and Individuals with Atypical Chromosome 22q11.2 Deletions Demonstrate the Crucial Role for Crkl in Craniofacial and Pharyngeal Development

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Molecular Syndromology, Vol. 5, Iss. 6, 2014-11 ,pp. : 276-286

Karger

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A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2–q22 linked to type 2 diabetes

By Dina C.  

Human Molecular Genetics, Vol. 12, Iss. 15, 2003-08 ,pp. : 1865-1873

Oxford University Press

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