Cite
HARVARD Citation
Boerkoel, P. et al. (2022). Long‐read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia. American journal of medical genetics. 188 (5), pp. 1589-1594. [Online].
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Boerkoel, P. et al. (2022). Long‐read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia. American journal of medical genetics. 188 (5), pp. 1589-1594. [Online].