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Carrier Assessment in Families with Lowe Oculocerebrorenal Syndrome: Novel Mutations in the OCRL1 Gene and Correlation of Direct DNA Diagnosis with Ocular Examination

✍ Scribed by Wulf Röschinger; Ania C. Muntau; Günther Rudolph; Adelbert A. Roscher; Stefan Kammerer

Book ID: 115639637
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 228 KB
Volume: 69
Category: Article
ISSN: 1096-7192
DOI: 10.1006/mgme.1999.2955

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