Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting
Irfan Saadi(University of Kansas Medical Center), Richard L. Maas(Tulane University), Wolfram Goessling(Brigham and Women's Hospital), James M. Harris(Beth Israel Deaconess Medical Center), Philippe Leboulch(Brigham and Women's Hospital), Stephen S. Gisselbrecht(Brigham and Women's Hospital), Aline Petrin(University of Iowa), Ursela Siddiqui(Brigham and Women's Hospital), Cynthia C. Morton(Brigham and Women's Hospital), Fowzan S. Alkuraya(Alfaisal University), Resy Cavallesco(Brigham and Women's Hospital), Jeffrey C. Murray(University of Iowa), Annick Turbé-Doan(Brigham and Women's Hospital), Hanne Hove(Copenhagen University Hospital), Arthur W. Grix(Kaiser Permanente), Robert P. Erickson(University of Arizona), Antônio Richieri‐Costa(Universidade de São Paulo), Thomas W. Glover(University of Michigan)
Cited by 96
Related Papers
<i>LMO2</i> -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
|Science|2003|3.5k
Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy
|Science|2009|1.5k
Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells.
|Proceedings of the National Academy of Sciences|1982|1.4k
Replicating genotype–phenotype associations
|Nature|2007|1.4k
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
|Nature Genetics|1994|1.3k