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European Journal of Human Genetics 2
Showing records 1 to 2 | Display all abstracts in European Journal of Human Genetics25410 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;
25409 Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
Tumer Z; Bach-Holm D
European Journal of Human Genetics 2009; 17: 1527-1539
