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Valter Augusto Della Rosa

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Indian Journal of Human Genetics|August 1, 2013
Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearingKarina Bezerra Salomão, Christiane Maria Ayo, Valter Augusto Della-Rosa
Codas|April 10, 2014
Distortion-product otoacoustic emissions at ultra-high frequencies in parents of individuals with autosomal recessive hearing lossJaqueline Medeiros de Mello, Valter Augusto Della-Rosa, Renata Mota Mamede Carvallo
Clinical Dysmorphology|May 11, 2002
DOOR syndrome: report of three additional casesTêmis Maria Félix, Simone de Menezes Karam, Valter Augusto Della Rosa, et al.
Drug and Chemical Toxicology|September 19, 2014
Genotoxic evaluation of terbinafine in human lymphocytes in vitroDanielle Tolomeotti, Marialba Avezum Alves de Castro-Prado, Juliane Rocha de Sant'Anna, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Indian Journal of Human Genetics|August 1, 2013
Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearingKarina Bezerra Salomão, Christiane Maria Ayo, Valter Augusto Della-Rosa
Codas|April 10, 2014
Distortion-product otoacoustic emissions at ultra-high frequencies in parents of individuals with autosomal recessive hearing lossJaqueline Medeiros de Mello, Valter Augusto Della-Rosa, Renata Mota Mamede Carvallo
Clinical Dysmorphology|May 11, 2002
DOOR syndrome: report of three additional casesTêmis Maria Félix, Simone de Menezes Karam, Valter Augusto Della Rosa, et al.
Drug and Chemical Toxicology|September 19, 2014
Genotoxic evaluation of terbinafine in human lymphocytes in vitroDanielle Tolomeotti, Marialba Avezum Alves de Castro-Prado, Juliane Rocha de Sant'Anna, et al.
Pageof 1