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Mendelsberg-Fishbein, Paola et al. Importancia del diagnóstico de mutaciones en el gen de la conexina 26 en el manejo integral de la sordera congénita no sindrómica. Bol. Med. Hosp. Infant. Mex., Abr 2013, vol.70, no.2, p.89-97. ISSN 1665-1146

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Cano-Hernández, Karla Sarahí et al. Prevalencia y espectro de las enfermedades que predisponen a la muerte súbita cardiaca en niños mexicanos: una muestra obtenida del Hospital Infantil de México Federico Gómez. Arch. Cardiol. Méx., Dic 2018, vol.88, no.4, p.268-276. ISSN 1405-9940

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