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Filtros : "Abramides, Dagma Venturini Marques" "Passos-Bueno, Maria Rita" Removidos: "SAÚDE BUCAL" "Anais do VII Encontro Científico de Pós-Graduação HRAC-USP" Limpar

Filtros

USP affiliated authors
- abramides, dagma venturini marques (~2)
- costa, antonio richieri da (~2)
- feniman, mariza ribeiro (~2)
- lamonica, dionisia aparecida cusin (~1)
- vitto, luciana paula maximino de (~1)
Date published
- 2010 (~1)
- 1998 (~1)
Subjects
- craniossinostose (1)
- diagnóstico por imagem (1)
- fatores de transcrição (1)
- genética (1)
- genética médica (1)

Artigo de periodico
Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a brazilian family (2010)
Lamônica, Dionísia Aparecida Cusin; Maximino, Luciana P.; Feniman, Mariza Ribeiro; Silva, Greyce K.; Zanchetta, Sthella; Abramides, Dagma Venturini Marques; Passos-Bueno, Maria Rita ; Rocha, Kátia; Richieri-Costa, Antonio
Source: The Cleft Palate-Craniofacial Journal. Unidades: FOB, HRAC
Subjects: CRANIOSSINOSTOSE, FATORES DE TRANSCRIÇÃO, MUTAÇÃO GENÉTICA, PERDA AUDITIVA NEUROSSENSORIAL, DIAGNÓSTICO POR IMAGEM, ORELHA MÉDIA (ESTRUTURA;ANOMALIAS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAMÔNICA, Dionísia Aparecida Cusin et al. Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a brazilian family. The Cleft Palate-Craniofacial Journal, v. 47, n. 5, p. Se 2010, 2010Tradução . . Disponível em: https://doi.org/10.1597/08-251.1. Acesso em: 10 nov. 2024.
APA
Lamônica, D. A. C., Maximino, L. P., Feniman, M. R., Silva, G. K., Zanchetta, S., Abramides, D. V. M., et al. (2010). Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a brazilian family. The Cleft Palate-Craniofacial Journal, 47( 5), Se 2010. doi:10.1597/08-251.1
NLM
Lamônica DAC, Maximino LP, Feniman MR, Silva GK, Zanchetta S, Abramides DVM, Passos-Bueno MR, Rocha K, Richieri-Costa A. Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a brazilian family [Internet]. The Cleft Palate-Craniofacial Journal. 2010 ; 47( 5): Se 2010.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1597/08-251.1
Vancouver
Lamônica DAC, Maximino LP, Feniman MR, Silva GK, Zanchetta S, Abramides DVM, Passos-Bueno MR, Rocha K, Richieri-Costa A. Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a brazilian family [Internet]. The Cleft Palate-Craniofacial Journal. 2010 ; 47( 5): Se 2010.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1597/08-251.1
Artigo de periodico
Speech/language findings in patients with Apert, Crouzon and Pfeiffer syndromes (1998)
Misquiatti, Andréa Regina N.; Abramides, Dagma Venturini Marques; Giacheti, Célia Maria; Feniman, Mariza Ribeiro; Passos-Bueno, Maria Rita ; Richieri-Costa, Antonio
Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidades: HRAC, FOB
Subjects: GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MISQUIATTI, Andréa Regina N. et al. Speech/language findings in patients with Apert, Crouzon and Pfeiffer syndromes. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 1, n. ja 1998, p. 29-35, 1998Tradução . . Acesso em: 10 nov. 2024.
APA
Misquiatti, A. R. N., Abramides, D. V. M., Giacheti, C. M., Feniman, M. R., Passos-Bueno, M. R., & Richieri-Costa, A. (1998). Speech/language findings in patients with Apert, Crouzon and Pfeiffer syndromes. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 1( ja 1998), 29-35.
NLM
Misquiatti ARN, Abramides DVM, Giacheti CM, Feniman MR, Passos-Bueno MR, Richieri-Costa A. Speech/language findings in patients with Apert, Crouzon and Pfeiffer syndromes. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( ja 1998): 29-35.[citado 2024 nov. 10 ]
Vancouver
Misquiatti ARN, Abramides DVM, Giacheti CM, Feniman MR, Passos-Bueno MR, Richieri-Costa A. Speech/language findings in patients with Apert, Crouzon and Pfeiffer syndromes. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1998 ; 1( ja 1998): 29-35.[citado 2024 nov. 10 ]

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