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Results: 1-3 |
Results: 3
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes
Authors: Splendore, A Silva, EO Alonso, LG Richieri-Costa, A Alonso, N Rosa, A Carakushanky, G Cavalcanti, DP Brunoni, D Passos-Bueno, MR
Citation: A. Splendore et al., High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes, HUM MUTAT, 16(4), 2000, pp. 315-322
Prenatal exposure to misoprostol and vascular disruption defects: A case-control study
Authors: Vargas, FR Schuler-Faccini, L Brunoni, D Kim, C Meloni, VFA Sugayama, SMM Albano, L Llerena, JC Almeida, JCC Duarte, A Cavalcanti, DP Goloni-Bertollo, E Conte, A Koren, G Addis, A
Citation: Fr. Vargas et al., Prenatal exposure to misoprostol and vascular disruption defects: A case-control study, AM J MED G, 95(4), 2000, pp. 302-306
Dandy-Walker malformation with postaxial polydactyly: Further evidence forautosomal recessive inheritance
Authors: Cavalcanti, DP Salomao, MA
Citation: Dp. Cavalcanti et Ma. Salomao, Dandy-Walker malformation with postaxial polydactyly: Further evidence forautosomal recessive inheritance, AM J MED G, 85(2), 1999, pp. 183-184
Risultati: 1-3 |