Sally Martell
AuthID: R-00G-A7Y
1
TÃTULO: Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2 Full Text
AUTORES: Jiadi Wen; Fatima Lopes; Gabriela Soares; Sandra A Farrell; Cara Nelson; Ying Qiao; Sally Martell; Chansonette Badukke; Carlos Bessa ; Bauke Ylstra; Suzanne Lewis; Nina Isoherranen; Patricia Maciel ; Evica Rajcan Separovic;
PUBLICAÇÃO: 2013, FONTE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 8, NÚMERO: 1
AUTORES: Jiadi Wen; Fatima Lopes; Gabriela Soares; Sandra A Farrell; Cara Nelson; Ying Qiao; Sally Martell; Chansonette Badukke; Carlos Bessa ; Bauke Ylstra; Suzanne Lewis; Nina Isoherranen; Patricia Maciel ; Evica Rajcan Separovic;
PUBLICAÇÃO: 2013, FONTE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 8, NÚMERO: 1
2
TÃTULO: Phenotypic and functional characterization of a recurrent microdeletion involving the 2p13.2 region Full Text
AUTORES: Jiadi D Wen; Fatima Lopes; Gabriela Soares; Sandra Farrell; Cara Nelson; Ying Qiao; Sally Martell; Chansonette Badukke; Teresa Temudo; Carlos Bessa; Bauke Ylstra; Suzanne Lewis; Nina Isoherranen; Patricia Marciel; Evica Rajcan Separovic;
PUBLICAÇÃO: 2013, FONTE: CHROMOSOME RESEARCH, VOLUME: 21
AUTORES: Jiadi D Wen; Fatima Lopes; Gabriela Soares; Sandra Farrell; Cara Nelson; Ying Qiao; Sally Martell; Chansonette Badukke; Teresa Temudo; Carlos Bessa; Bauke Ylstra; Suzanne Lewis; Nina Isoherranen; Patricia Marciel; Evica Rajcan Separovic;
PUBLICAÇÃO: 2013, FONTE: CHROMOSOME RESEARCH, VOLUME: 21
INDEXADO EM: 
WOS
WOS