Genética clínica (2014)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; CEIDE, ROSELI MARIA ZECHI - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC ; ALVAREZ, CAMILA WENCESLAU - HRAC
- Unidade: HRAC
- Subjects: GENÉTICA; ANORMALIDADES CRANIOFACIAIS; HOSPITAIS
- Language: Português
- Imprenta:
- Publisher: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais
- Publisher place: Bauru
- Date published: 2014
- Source:
- Conference titles: Curso de Anomalias Congênitas Labiopalatinas
-
ABNT
RICHIERI-COSTA, Antonio; GUION-ALMEIDA, Maria Leine; NAKATA, Nancy Mizue Kokitsu; et al. Genética clínica. Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2014. -
APA
Richieri-Costa, A., Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., Pittoli, S. V. P., & Alvarez, C. W. (2014). Genética clínica. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. -
NLM
Richieri-Costa A, Guion-Almeida ML, Nakata NMK, Ceide RMZ, Pittoli SVP, Alvarez CW. Genética clínica. Anais. 2014 ; -
Vancouver
Richieri-Costa A, Guion-Almeida ML, Nakata NMK, Ceide RMZ, Pittoli SVP, Alvarez CW. Genética clínica. Anais. 2014 ; - Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients
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- Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients
- 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
- Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings
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