DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Vaclavik V, Schorderet DF, Borruat FX, Munier FL.
Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutation.
Ophthalmic Genet 2011;
32 (2) 114-117
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