DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Williamson KA, Rainger J, Floyd JA , et al; UK10K Consortium.
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Am J Hum Genet 2014;
94 (2) 295-302
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