Browsing by Author Kok, F.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 6 to 8 of 8 < previous 
Issue DateTitleAuthor(s)
1-Dec-2000Prader-Willi syndrome: Genetic tests and clinical findingsFridman, C.; Varela, M. C.; Kok, F.; Setian, N.; Koiffmann, C. P.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Dec-2005Vitamin B-12 deficiency in infancy as a cause of developmental regressionCasella, E. B.; Valente, M.; Navarro, J. M. de; Kok, F.; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP)
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 6 to 8 of 8 < previous