Jaffe–Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder-Reference-Cited by-同舟云学术

Jaffe–Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

Published:2014-06 Issue:6 Volume:16 Page:448-459
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

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,Messiaen Ludwine

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2013163.pdf

Reference43 articles.

1. Disseminated nonossifying fibromas in association with café-au-lait spots (Jaffe-Campanacci syndrome).;Mirra;Clin Orthop Relat Res,1982

2. Tumors and Tumorous Conditions of the Bones and Joints.;Jaffe,1958

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