APA

Stewart D. R., Brems H., Gomes A. G., Ruppert S. L., Callens T., Williams J., Claes K., Bober M. B., Hachen R., Kaban L. B., Li H., Lin A., McDonald M., Melancon S., Ortenberg J., Radtke H. B., Samson I., Saul R. A., Shen J., Siqveland E., Toler T. L., van Maarle M., Wallace M., Williams M., Legius E. & Messiaen L. (20150512). Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. : Genetics in medicine : official journal of the American College of Medical Genetics.

Chicago

Stewart Douglas R, Brems Hilde, Gomes Alicia G, Ruppert Sarah L, Callens Tom, Williams Jennifer, Claes Kathleen, Bober Michael B, Hachen Rachel, Kaban Leonard B, Li Hua, Lin Angela, McDonald Marie, Melancon Serge, Ortenberg June, Radtke Heather B, Samson Ignace, Saul Robert A, Shen Joseph, Siqveland Elizabeth, Toler Tomi L, van Maarle Merel, Wallace Margaret, Williams Misti, Legius Eric and Messiaen Ludwine. 20150512. Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. : Genetics in medicine : official journal of the American College of Medical Genetics.

Harvard

Stewart D. R., Brems H., Gomes A. G., Ruppert S. L., Callens T., Williams J., Claes K., Bober M. B., Hachen R., Kaban L. B., Li H., Lin A., McDonald M., Melancon S., Ortenberg J., Radtke H. B., Samson I., Saul R. A., Shen J., Siqveland E., Toler T. L., van Maarle M., Wallace M., Williams M., Legius E. and Messiaen L. (20150512). Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. : Genetics in medicine : official journal of the American College of Medical Genetics.

MLA

Stewart Douglas R, Brems Hilde, Gomes Alicia G, Ruppert Sarah L, Callens Tom, Williams Jennifer, Claes Kathleen, Bober Michael B, Hachen Rachel, Kaban Leonard B, Li Hua, Lin Angela, McDonald Marie, Melancon Serge, Ortenberg June, Radtke Heather B, Samson Ignace, Saul Robert A, Shen Joseph, Siqveland Elizabeth, Toler Tomi L, van Maarle Merel, Wallace Margaret, Williams Misti, Legius Eric and Messiaen Ludwine. Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. : Genetics in medicine : official journal of the American College of Medical Genetics. 20150512.