Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA) - Funari, Mariana F. A.; Jorge, Alexander A. L.; Pinto, Emilia M.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Nishi, Mirian Y. (Arquivos Brasileiros de Endocrinologia e Metabologia, 2008)