Not logged inKinetic inductance traveling-wave amplifiers for multiplexed qubit readout
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SaveShare Save Share Save Share Save Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial CleftingSaadi, Irfan; Alkuraya, Fowzan S.; Gisselbrecht, Stephen S.; Goessling, Wolfram; Cavallesco, Resy; Turbe-Doan, Annick; Petrin, Aline L.; Harris, James; Siddiqui, Ursela; Grix, Arthur W., Jr.; Hove, Hanne D.; Leboulch, Philippe; Glover, Thomas W.; Morton, Cynthia C.; Richieri-Costa, Antonio; Murray, Jeffrey C.; Erickson, Robert P.; Maas, Richard L. Share Save Share Save Share Save Share Save Share Save Share Save Share Save Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeFang, JM; Dagenais, SL; Erickson, RP; Arlt, MF; Glynn, MW; Gorski, JL; Seaver, LH; Glover, TW Share Save Share Save Share Save 
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