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Human Molecular Genetics, Vol. 7, Iss. 9, 1998-09 ,pp. : 1363-1369

Oxford University Press

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The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome

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Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

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Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 915-922

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Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndrome

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Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 405-413

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Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith–Magenis syndrome

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