(Q50866527)
Statements
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Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern. (English)
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Ogata T
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Wakui K
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Muroya K
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Ohashi H
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Matsuo N
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Brown DM
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Ishii T
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Fukushima Y
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1 July 1998
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103
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1
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51-56
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