@inproceedings{inproceedingsd162e86d,
title   = {OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD)},
author = {Novaretti, Nathalia and Santos, Paulo S. and Moreira, Ayrton Custódio and Martinelli Junior, Carlos Eduardo and Igarashi, M. and Ogata, T. and Fukami, M. and Castro, Margaret de and Antonini, Sonir Roberto Rauber},
year = {2013},
publisher = {SBP},
booktitle   = {Congresso Brasileiro Pediátrico de Endocrinologia e Metabologia}
}