Browsing by Author Gonzalez, C. H.

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Showing results 1 to 12 of 12
Issue DateTitleAuthor(s)
1-May-2000AEC syndrome and CHAND syndrome: Further evidence of clinical overlapping in the ectodermal dysplasiasBertola, D. R.; Kim, C. A.; Sugayama, SMM; Albano, LMJ; Utagawa, C. Y.; Gonzalez, C. H.; Universidade Federal de São Paulo (UNIFESP)
22-Jan-2001Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?Bertola, D. R.; Kim, C. A.; Pereira, A. C.; Mota, GFA; Krieger, J. E.; Vieira, I. C.; Valente, M.; Loreto, M. R.; Magalhaes, R. P.; Gonzalez, C. H.; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP)
1-Jan-1983CHONDROECTODERMAL DYSPLASIA (ELLIS-VANCREVELD) WITH ANOMALIES of CNS and URINARY-TRACTRosemberg, S.; Carneiro, P. C.; Zerbini, MCN; Gonzalez, C. H.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Jan-1985CREATINE-KINASE and PYRUVATE-KINASE ACTIVITIES in NORMAL-CHILDREN - IMPLICATIONS in DUCHENNE MUSCULAR-DYSTROPHY CARRIER DETECTIONPassos, M. R.; Gonzalez, C. H.; Zatz, M.; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP)
1-Jan-1984FIBROCHONDROGENESIS - LETHAL, AUTOSOMAL RECESSIVE CHONDRODYSPLASIA WITH DISTINCTIVE CARTILAGE HISTOPATHOLOGYWhitley, C. B.; Langer, L. O.; Ophoven, J.; Gilbert, E. F.; Gonzalez, C. H.; Mammel, M.; Coleman, M.; Rosemberg, S.; Rodriques, C. J.; Sibley, R.; Horton, W. A.; Opitz, J. M.; Gorlin, R. J.; CHILDRENS HOSP; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP); UNIV TEXAS; SHODAIR CHILDRENS HOSP; UNIV WISCONSIN; UNIV MINNESOTA
1-Feb-2000Further delineation of Char syndromeBertola, D. R.; Kim, CAE; Sugayama, SMM; Utagawa, C. Y.; Albano, LMJ; Gonzalez, C. H.; Universidade Federal de São Paulo (UNIFESP)
15-Sep-1993HUMAN SITUS DETERMINATION and CHROMOSOME CONSTITUTION 46,XY,INS(7-8)(Q22-Q12Q24)Koiffmann, C. P.; Wajntal, A.; Desouza, D. H.; Gonzalez, C. H.; Coates, M. V.; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP)
1-May-1991IS SHWACHMAN SYNDROME (MCKUSICK-26040) A CHROMOSOME BREAKAGE SYNDROMEKoiffmann, C. P.; Gonzalez, C. H.; Souza, D. H.; Romani, E. G.; Kim, C. A.; Wajntal, A.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Aug-1993LIMB DEFICIENCY WITH OR WITHOUT MOBIUS SEQUENCE in 7 BRAZILIAN CHILDREN ASSOCIATED WITH MISOPROSTOL USE in the 1ST TRIMESTER of PREGNANCYGonzalez, C. H.; Vargas, F. R.; Perez, ABA; Kim, C. A.; Brunoni, D.; Marquesdias, M. J.; Leone, C. R.; Neto, J. C.; Llerena, J. C.; Dealmeida, JCC; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP); FIOCRUZ MS
1-Dec-2003Mobius sequence in children exposed in utero to misoprostol: Neuropathological study of three casesMarques-Dias, M. J.; Gonzalez, C. H.; Rosemberg, S.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
31-Jul-1995NEUROBLASTOMA in A BOY WITH MCA/MR SYNDROME, DELETION 11Q, and DUPLICATION 12QKoiffmann, C. P.; Gonzalez, C. H.; Viannamorgante, A. M.; Kim, C. A.; ODONE, V; Wajntal, A.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Jan-1981PATHOLOGIC FINDINGS in the WOLF-HIRSCHHORN (4P-) SYNDROMEGonzalez, C. H.; Capelozzi, V. L.; Wajntal, A.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)