Associated Papers
New insights into the phenotypic spectrum of 14q22q23 deletions: a case report and literature review.
Pichiecchio A et al.
Bmc Medical Genomics, 2018
A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.
Lonero A et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2016
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