Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients (2015)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; CEIDE, ROSELI MARIA ZECHI - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC ; ALVAREZ, CAMILA WENCESLAU - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- Subjects: GENÉTICA MÉDICA; HIPERTELORISMO; FISSURA LÁBIOPALATINA
- 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
RICHIERI-COSTA, Antonio et al. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 29 dez. 2025. -
APA
Richieri-Costa, A., Migliore, C., Meroni, G., Siemann, M. E., Zechi-Ceide, R. M., Nakata, N. M. K., et al. (2015). Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index -
NLM
Richieri-Costa A, Migliore C, Meroni G, Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Alvarez CW, Guion-Almeida ML. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients [Internet]. Final Program. 2015 ;[citado 2025 dez. 29 ] Available from: http://www.ecc2015.se/author-index -
Vancouver
Richieri-Costa A, Migliore C, Meroni G, Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Alvarez CW, Guion-Almeida ML. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients [Internet]. Final Program. 2015 ;[citado 2025 dez. 29 ] Available from: http://www.ecc2015.se/author-index - Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis
- Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum
- Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients
- Genética clínica
- Microcephaly, cleft lip/palate and intellectual disabilities in siblings. A new familial case of Richieri-Costa/Guion Almeida syndrome type 1?
- Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings
- 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
- Atypical phenotype of Opitz GBBB syndrome caused by a novel mid1 variation
- O serviço de genética no HRAC-USP
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