DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

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

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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