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Results: 1-5 |
Results: 5

Authors: SCHWEITZER DN PRZYLEPA KA GRAHAM JM LACHMAN RS JABS EW
Citation: Dn. Schweitzer et al., SUBTLE RADIOGRAPHIC FINDINGS IN CROUZON-SYNDROME WITH ACANTHOSIS NIGRICANS, Journal of investigative medicine, 46(1), 1998, pp. 120-120

Authors: FILKINS K RUSSO JF BOEHMER S CAMOUS M PRZYLEPA KA JIANG W JABS EW
Citation: K. Filkins et al., PRENATAL ULTRASONOGRAPHIC AND MOLECULAR DIAGNOSIS OF APERT-SYNDROME, Prenatal diagnosis, 17(11), 1997, pp. 1081-1084

Authors: PRZYLEPA KA PAZNEKAS W ZHANG MH GOLABI M BIAS W BAMSHAD MJ CAREY JC HALL BD STEVENSON R ORLOW SJ COHEN MM JABS EW
Citation: Ka. Przylepa et al., FIBROBLAST GROWTH-FACTOR RECEPTOR-2 MUTATIONS IN BEARE-STEVENSON CUTIS GYRATA SYNDROME, Nature genetics, 13(4), 1996, pp. 492-494

Authors: MEYERS GA DAY D GOLDBERG R DAENTL DL PRZYLEPA KA ABRAMS LJ GRAHAM JM FEINGOLD M RAWNSLEY E SCOTT AF JABS EW
Citation: Ga. Meyers et al., FCFR2 EXON IIIA AND IIIE MUTATIONS IN CROUZON, JACKSON-WEISS, AND PFEIFFER SYNDROMES - EVIDENCE FOR MISSENSE CHANGES, INSERTIONS, AND A DELETION DUE TO ALTERNATIVE RNA SPLICING, American journal of human genetics, 58(3), 1996, pp. 491-498

Authors: MEYERS GA ORLOW SJ MUNRO IR PRZYLEPA KA JABS EW
Citation: Ga. Meyers et al., FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 (FGFR3) TRANSMEMBRANE MUTATION INCROUZON-SYNDROME WITH ACANTHOSIS NIGRICANS, Nature genetics, 11(4), 1995, pp. 462-464
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