Associated Papers
Genetic architecture of retinoic-acid signaling-associated ocular developmental defects.
Nedelec B et al.
Human Genetics, 2019
Novel STRA6 null mutations in the original family described with Matthew-Wood syndrome.
Pasutto F et al.
American Journal of Medical Genetics. Part A, 2018
Exome sequencing in 32 patients with anophthalmia/microphthalmia and developmental eye defects.
Slavotinek AM et al.
Clinical Genetics, 2015
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