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HARVARD Citation
Pölsler, L. et al. (2020). A Syrian patient with Steel syndrome due to compound heterozygous COL27A1 mutations with colobomata of the eye. American journal of medical genetics. 182 (4), pp. 730-734. [Online].
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Pölsler, L. et al. (2020). A Syrian patient with Steel syndrome due to compound heterozygous COL27A1 mutations with colobomata of the eye. American journal of medical genetics. 182 (4), pp. 730-734. [Online].