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Schrooyen M 1

Showing records 1 to 1 | Display all abstracts from Schrooyen M

25410 LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma
Desir J; Sznajer Y; Depasse F; Roulez F; Schrooyen M; Meire F; Abramowicz M
European Journal of Human Genetics 2010;

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