Browsing by Author Bertola, D. R.

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Issue DateTitleAuthor(s)
1-Jun-2012Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?Bertola, D. R.; Pereira, A. C.; Brasil, A. S.; Suzuki, L.; Leite, C.; Falzoni, R.; Tannuri, U.; Poplawski, A. B.; Janowski, K. M.; Kim, C. A.; Messiaen, L. M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP); Univ Alabama Birmingham
2018Richieri-Costa-Pereira syndrome: Expanding its phenotypic and genotypic spectrumBertola, D. R.; Hsia, G.; Alvizi, L.; Gardham, A.; Wakeling, E. L.; Yamamoto, G. L.; Honjo, R. S.; Oliveira, L. A. N.; Di Francesco, R. C.; Perez, B. A. [UNIFESP]; Kim, C. A.; Passos-Bueno, M. R.
1-Jan-2006Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsKrepischi-Santos, A. C. V.; Vianna-Morgante, A. M.; Jehee, F. S.; Passos-Bueno, M. R.; Knijnenburg, J.; Szuhai, K.; Sloos, W.; Mazzeu, J. F.; Kok, F.; Cheroki, C.; Otto, P. A.; Mingroni-Netto, R. C.; Varela, M.; Koiffmann, C.; Kim, C. A.; Bertola, D. R.; Pearson, P. L.; Rosenberg, C.; Universidade de São Paulo (USP); Leiden Univ; Universidade Federal de São Paulo (UNIFESP); Robinow Syndrome Fdn
Showing results 5 to 7 of 7 < previous