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Title:	Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1
Source:	Human Molecular Genetics [0964-6906] Wat, M J yr:2012

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description	19.	Dickson, Dennis W W. "Progressive supranuclear palsy: pathology and genetics." Brain pathology 17.1 (2006): 74-82.
description	20.	Flores, M. "Recurrent DNA inversion rearrangements in the human genome." Proceedings of the National Academy of Sciences of the United States of America 104.15 (2007): 6099-6106.