Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis (2015)
- Authors:
- USP affiliated authors: ALVAREZ, CAMILA WENCESLAU - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; CEIDE, ROSELI MARIA ZECHI - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Subjects: EVOLUÇÃO FENOTÍPICA; FISSURA LÁBIOPALATINA; HIPERTELORISMO
- 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
ALVAREZ, Camila Wenceslau et al. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 28 dez. 2025. -
APA
Alvarez, C. W., Guion-Almeida, M. L., Rafacho, M. B., Nakata, N. M. K., Zechi-Ceide, R. M., Pittoli, S. V. P., et al. (2015). Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index -
NLM
Alvarez CW, Guion-Almeida ML, Rafacho MB, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Meroni G, Richieri-Costa A. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis [Internet]. Final Program. 2015 ;[citado 2025 dez. 28 ] Available from: http://www.ecc2015.se/author-index -
Vancouver
Alvarez CW, Guion-Almeida ML, Rafacho MB, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Meroni G, Richieri-Costa A. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis [Internet]. Final Program. 2015 ;[citado 2025 dez. 28 ] Available from: http://www.ecc2015.se/author-index - Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients
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- Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings
- Atypical phenotype of Opitz GBBB syndrome caused by a novel mid1 variation
- Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3
- Genética clínica no HRAC-USP
- O serviço de genética no HRAC-USP
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