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de Vos IJ 1
Showing records 1 to 1 | Display all abstracts from de Vos IJ67569 The 6p25 deletion syndrome: An update on a rare neurocristopathy
de Vos IJ; Stegmann AP; Webers CA; Stumpel CT
Ophthalmic Genetics 2016; 0: 1-7
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