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: 27 dez. 2025. -
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 2025 dez. 27 ] 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 2025 dez. 27 ] Available from: http://www.ecc2015.se/author-index - Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
- Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding
- O serviço de genética clínica no HRAC/USP
- O serviço de genética clínica no HRAC-USP
- A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
- Espectro oculoauriculovertebral: relato de 5 casos familiais com herança autossômica dominante
- Microcephaly, cleft lip/palate and intellectual disabilities in siblings. A new familial case of Richieri-Costa/Guion Almeida syndrome type 1?
- Caracterização do espectro fenotípico de pacientes com fissuras labiopalatinas associadas a múltiplas anomalias congênitas e alterações cromossômicas estruturais
- O serviço de genética no HRAC-USP
- O Serviço de Genética Clínica no HRAC-USP
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
