Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki–Lupski duplication syndrome

By Sun Zhe   Liu Pengfei   Jia Xueyuan   Withers Marjorie A.   Jin Li   Lupski James R.   Zhang Feng  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 749-756

Oxford University Press

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Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome

By Till Sally M.   Wijetunge Lasani S.   Seidel Viktoria G.   Harlow Emily   Wright Ann K.   Bagni Claudia   Contractor Anis   Gillingwater Thomas H.   Kind Peter C.  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2143-2156

Oxford University Press

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The 3A subunit gene ( Ap3b1 ) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky–Pudlak syndrome and night blindness

By Eicher E.M.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 323-330

Oxford University Press

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Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

By Moretti Paolo   Bouwknecht J. Adriaan   Teague Ryan   Paylor Richard   Zoghbi Huda Y.  

Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 205-220

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Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease

By Pang Terence Y.C.   Du Xin   Zajac Michelle S.   Howard Monique L.   Hannan Anthony J.  

Human Molecular Genetics, Vol. 18, Iss. 4, 2009-02 ,pp. : 753-766

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