Phenotype–genotype correlations and emerging pathways in ocular anterior segment dysgenesis
Author:
Funder
National Health and Medical Research Council
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-018-1935-7.pdf
Reference144 articles.
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4. Aliferis K et al (2010) A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly. Ophthalmic Genet 31:205–208. https://doi.org/10.3109/13816810.2010.512355
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