Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination.

MLA

Röschinger, W., et al. “Carrier Assessment in Families with Lowe Oculocerebrorenal Syndrome: Novel Mutations in the OCRL1 Gene and Correlation of Direct DNA Diagnosis with Ocular Examination.” Molecular Genetics and Metabolism, vol. 69, no. 3, Mar. 2000, pp. 213–22. EBSCOhost, https://doi.org/10.1006/mgme.1999.2955.

APA

Röschinger, W., Muntau, A. C., Rudolph, G., Roscher, A. A., & Kammerer, S. (2000). Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination. Molecular Genetics and Metabolism, 69(3), 213–222. https://doi.org/10.1006/mgme.1999.2955

Chicago

Röschinger, W, A C Muntau, G Rudolph, A A Roscher, and S Kammerer. 2000. “Carrier Assessment in Families with Lowe Oculocerebrorenal Syndrome: Novel Mutations in the OCRL1 Gene and Correlation of Direct DNA Diagnosis with Ocular Examination.” Molecular Genetics and Metabolism 69 (3): 213–22. doi:10.1006/mgme.1999.2955.