Sally Martell
AuthID: R-00G-A7Y
1
TITLE: Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2 Full Text
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 8, ISSUE: 1
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 8, ISSUE: 1
2
TITLE: Phenotypic and functional characterization of a recurrent microdeletion involving the 2p13.2 region Full Text
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: CHROMOSOME RESEARCH, VOLUME: 21
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: CHROMOSOME RESEARCH, VOLUME: 21
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