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bibliographicCitation Roessler E, Ma Y, Ouspenskaia MV, Lacbawan F, Bendavid C, Dubourg C, Beachy PA, Muenke M. Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans. Human Genetics. 2009 Jan 31;125(4):393–400. doi: 10.1007/s00439-009-0628-7.
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date 2009-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language English
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title Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans
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Total number of triples: 39.