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Search on : LEZIROVITZ, KARINA [Author]
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 Pupo, Altair Cadrobbi et al. Estudo de família brasileira portadora de deficiência auditiva sensorioneural não-sindrômica com herança mitocondrial. Rev. Bras. Otorrinolaringol., Out 2008, vol.74, no.5, p.786-789. ISSN 0034-7299

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 Mazzeu, Juliana F. et al. Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes. Genet. Mol. Biol., Mar 2007, vol.30, no.2, p.339-342. ISSN 1415-4757
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 Pardono, Eliete et al. Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant. Genet. Mol. Biol., 2006, vol.29, no.4, p.601-604. ISSN 1415-4757
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 Pelegrino, Karla de Oliveira et al. MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization. Clinics, Aug 2012, vol.67, no.8, p.981-985. ISSN 1807-5932
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