Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Patrícia R. de M. Lima"'
Autor:
Patrícia P.O. Rocha, Juliana G. Giannetti, Marzia Pollazzon, Alessandro Iodice, Maria Marinelli, Satz Mengensatzproduktion, Ilaria Kolobova, Elvis C. Mateo, Patrícia R. de M. Lima, Manuela Napoli, Ivan Ivanovski, Tiong Yang Tan, Martin Poot, Elga Fabia Belligni, Joziele de S. Lima, Siulan Vendramini-Pittoli, Livia Garavelli, Rafaella X. Pietra, Bruno F. Gamba, Carlo Fusco, Charles Coutton, Veronica Barbieri, Giovana da C. César, Roseli Maria Zechi-Ceide, Mariana Lacerda de Freitas, Luana Assis Ferreira, Paula Frassinetti Vasconcelos de Medeiros, Gabrielle S. Vianna, Michele da S. Gonçalves, Nicky Kilpatrick, Francesca Madia, Anthony J. Penington, Chiara Sartori, Jessie X. Xu, Nancy Mizue Kokitsu-Nakata, Manuela Mussini, Fernanda S. Jehee, Fabrizia Franchi, Maria E. Street, Carla Rosenberg, Patrick Yap, Liam Crapper, Antonio Richieri-Costa, Rejane A.C. Monteiro, Rosana R. Xavier, Ilenia Maini, Naomi L. Baker, Scott C. Bell, Maria Augusta N.P. Monteiro, Valdirene T. de Oliveira, Simonetta Rosato, Ana C.V. Krepischi Santos, Druckerei Stückle, Carl Ernst, Rosario Pascarella, Andréia M. Carvalho, Lucilene Arilho Ribeiro-Bicudo, Peter G. Farlie
Publikováno v:
Molecular Syndromology. 7:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db58d86090fdaf131c3502e161f58fd5
https://doi.org/10.1159/000452981
https://doi.org/10.1159/000452981
Autor:
Rejane A.C. Monteiro, Mariana Lacerda de Freitas, Rosana R. Xavier, Patrícia P.O. Rocha, Fernanda Sarquis Jehee, Juliana G. Giannetti, Paula Frassinetti Vasconcelos de Medeiros, Maria Augusta N.P. Monteiro, Michele da S. Gonçalves, Luana Assis Ferreira, Gabrielle S. Vianna, Giovana da C. César, Rafaella X. Pietra, Valdirene T. de Oliveira, Elvis C. Mateo, Joziele de S. Lima, Patrícia R. de M. Lima, Andreia Carvalho
Publikováno v:
Molecular syndromology. 7(6)
Chromosomal changes are frequently observed in patients with syndromic seizures. Understanding the genetic etiology of this pathology is crucial for the guidance and genetic counseling of families as well as for the establishment of appropriate treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14fdd8a9dc7433c7c07088c98b711c14
https://pubmed.ncbi.nlm.nih.gov/27920636
https://pubmed.ncbi.nlm.nih.gov/27920636