Associated Papers
[Clinical and genetic results with reference to corneal alterations in Lowe-syndrome].
Rudolph G et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft, 2004
Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination.
Röschinger W et al.
Molecular Genetics and Metabolism, 2000
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