In the article “The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1”1 in the January/February 2003 issue of Genetics in Medicine, the names of Ekaterina Tsilou, MD and Benjamin I. Rubin, MD, of the National Eye Institute, National Institutes of Health, Baltimore, Maryland, was unintentionally omitted from the list of authors. The authors regret this omission.
Reference
Liberfarb RM, Levy HP, Rose PS, Wilkin DJ, Davis J, Balog JZ, Griffith AJ, Szymko-Bennett YM, Johnston JJ, Tsilous E, Rubin BI, Francomano CA The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1. Genet Med 2003; 5: 21–27.
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The online version of the original article can be found at 10.1097/00125817-200301000-00004
The online version of the original article can be found at 10.1097/01.GIM.0000086479.80559.EA
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Erratum. Genet Med 5, 478 (2003). https://doi.org/10.1097/00125817-200311000-00011
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DOI: https://doi.org/10.1097/00125817-200311000-00011
