Cite
HARVARD Citation
Reis, L. et al. (2016). Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies. Clinical genetics. 90 (4), pp. 378-382. [Online].
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Reis, L. et al. (2016). Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies. Clinical genetics. 90 (4), pp. 378-382. [Online].