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Milena Simioni de Carvalho

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Universidade Estadual de Campinas (UNICAMP). Faculdade de Ciências Médicas (FCM)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

Milena Simioni de Carvalho in research grants and scholarships supported by FAPESP.

Scholarships in Brazil
FAPESP support in numbers * Updated May 30, 2020
Total / Available in English
2 / 1 Completed scholarships in Brazil

Associated processes
Most frequent collaborators in research granted by FAPESP
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Use this Research Supported by FAPESP (BV/FAPESP) channel only to send messages referring to FAPESP-funded scientific projects.





Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (3)

(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)

Data from Web of Science

FONTES, MARSHALL I. B.; SANTOS, ANA P.; MOLCK, MIRIAM C.; SIMIONI, MILENA; NASCIMENTO, DIOGO L. L.; ANDRADE, ANA K. M.; ROSENBERG, CARLA; KREPISCHI, ANA C. V.; APPENZELLER, SIMONE; MONLLEO, ISABELLA L.; et al. Genotype-Phenotype Correlation of 16p13.3 Terminal Duplication and 22q13.33 Deletion: Natural History of a Patient and Review of the Literature. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 170, n. 3, p. 766-772, . Web of Science Citations: 3. (12/10071-0, 09/00898-1, 12/51799-6, 13/08028-1)

SIMIONI, MILENA; STEINER, CARLOS EDUARDO; GIL-DA-SILVA-LOPES, VERA LUCIA. De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case. Gene, v. 573, n. 1, p. 166-170, . Web of Science Citations: 4. (12/10071-0, 11/23794-7)

SIMIONI, MILENA; ARTIGUENAVE, FRANCOIS; MEYER, VINCENT; SGARDIOLI, ILARIA C.; VIGUETTI-CAMPOS, NILMA L.; MONLLEO, ISABELLA LOPES; MACIEL-GUERRA, ANDREA T.; STEINER, CARLOS E.; GIL-DA-SILVA-LOPES, VERA L.. Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes. MOLECULAR SYNDROMOLOGY, v. 8, n. 4, p. 187-194, . Web of Science Citations: 1. (12/10071-0, 11/23794-7)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

CARVALHO, Milena Simioni de. Investigação da região 22q11.2 em defeitos de linha media facial com hipertelorismo. Dissertação (Mestrado) -  Faculdade de Ciências Médicas.  Universidade Estadual de Campinas (UNICAMP).  (05/03555-7

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