An unusual association between craniosynostosis and OAVS: report on two cases (2013)
- Authors:
- USP affiliated authors: NAKATA, NANCY MIZUE KOKITSU - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC
- Unidade: HRAC
- Subjects: ANORMALIDADES CRANIOFACIAIS; CRANIOSSINOSTOSE; GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais
- Publisher place: Bauru
- Date published: 2013
- Source:
- Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas
-
ABNT
SANTOS, J. M. e NAKATA, Nancy Mizue Kokitsu e PITTOLI, Siulan Vendramini Paulovich. An unusual association between craniosynostosis and OAVS: report on two cases. 2013, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013. Disponível em: https://repositorio.usp.br/directbitstream/9820175e-1c4b-4b78-9d6b-b8f13ff49d17/2513963.pdf. Acesso em: 16 abr. 2024. -
APA
Santos, J. M., Nakata, N. M. K., & Pittoli, S. V. P. (2013). An unusual association between craniosynostosis and OAVS: report on two cases. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/9820175e-1c4b-4b78-9d6b-b8f13ff49d17/2513963.pdf -
NLM
Santos JM, Nakata NMK, Pittoli SVP. An unusual association between craniosynostosis and OAVS: report on two cases [Internet]. Anais. 2013 ;[citado 2024 abr. 16 ] Available from: https://repositorio.usp.br/directbitstream/9820175e-1c4b-4b78-9d6b-b8f13ff49d17/2513963.pdf -
Vancouver
Santos JM, Nakata NMK, Pittoli SVP. An unusual association between craniosynostosis and OAVS: report on two cases [Internet]. Anais. 2013 ;[citado 2024 abr. 16 ] Available from: https://repositorio.usp.br/directbitstream/9820175e-1c4b-4b78-9d6b-b8f13ff49d17/2513963.pdf - Fissura de palato, microstomia e micrognatia de herança autossômica dominante: ligação com o sítio frágil do 16q22?
- A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
- Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
- Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome
- Espectro oculoauriculovertebral: relato de 5 casos familiais com herança autossômica dominante
- Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding
- Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
- Audiological findings in patients with the Richieri-Costa-Pereira syndrome
- Estudo genético-clínico de 144 pacientes portadores de deficiência auditiva não sindrômica
- Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 | 2513963.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
