Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP (2015)
- Authors:
- USP affiliated authors: CEIDE, ROSELI MARIA ZECHI - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC
- Unidade: HRAC
- Subjects: GENÉTICA; HOSPITAIS; SÍNDROME DE PIERRE ROBIN
- Language: Inglês
- Imprenta:
- Publisher: European Cleft Plate and Craniofacial Association
- Publisher place: Gothenburg
- Date published: 2015
- Source:
- Título: Final Program
- Conference titles: European Craniofacial Congress
-
ABNT
ZECHI-CEIDE, Roseli Maria et al. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 03 out. 2024. -
APA
Zechi-Ceide, R. M., Guion-Almeida, M. L., Nakata, N. M. K., & Pittoli, S. V. P. (2015). Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index -
NLM
Zechi-Ceide RM, Guion-Almeida ML, Nakata NMK, Pittoli SVP. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP [Internet]. Final Program. 2015 ;[citado 2024 out. 03 ] Available from: http://www.ecc2015.se/author-index -
Vancouver
Zechi-Ceide RM, Guion-Almeida ML, Nakata NMK, Pittoli SVP. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP [Internet]. Final Program. 2015 ;[citado 2024 out. 03 ] Available from: http://www.ecc2015.se/author-index - Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding
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