Isocromosoma Xq en mosaico y microduplicación 17pl3.3pl3.2 en una paciente con síndrome de Turner y catarata congénita
Rojas Martínez, Jorge A; Acosta Guio, Johanna C.
Arch. argent. pediatr
; 113(1): e21-e25, ene. 2015.
Artículo en Español | BINACIS | ID: bin-132033
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