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Bruno Faulin Gamba

CV Lattes


Universidade de São Paulo (USP). Hospital de Reabilitação de Anomalias Craniofaciais (HRAC)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

bachelor's at Ciências Biológicas from Universidade Estadual do Norte do Paraná (2007), master's at Pós-Graduação em Ciências Biológicas from Universidade Estadual Paulista, Botucatu (2010) and doctorate at Genética from Instituto de Biociências de Botucatu (2015). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: smith-magenis syndrome, fish, citogenética vegetal, citogenética animal and mlpa. (Source: Lattes Curriculum)

News published in Agência FAPESP Newsletter about the researcher
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VEICULO: TITULO (DATA)
VEICULO: TITULO (DATA)
FAPESP support in numbers * Updated November 27, 2021
Total / Available in English
1 / 1   Completed scholarships in Brazil

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Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (2)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

Publications2
Citations9
Cit./Article4.5
Data from Web of Science

GAMBA, BRUNO FAULIN; RICHIERI-COSTA, ANTONIO; COSTA, SILVIA; ROSENBERG, CARLA; RIBEIRO-BICUDO, LUCILENE ARILHO. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, v. 290, n. 6, p. 2213-2216, . Web of Science Citations: 8. (11/07012-9, 10/18740-2)

GAMBA, BRUNO F.; ROSENBERG, CARLA; COSTA, SILVIA; RICHIERI-COSTA, ANTONIO; RIBEIRO-BICUDO, LUCILENE A.. Cleft Lip/Palate, Short Stature, and Developmental Delay in a Boy with a 5.6-Mb Interstitial Deletion Involving 10p15.3p14. MOLECULAR SYNDROMOLOGY, v. 6, n. 1, p. 39-43, . Web of Science Citations: 1. (11/07012-9, 10/18740-2)

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