Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group

Infantile myofibromatosis (IM), which is typically diagnosed in young children, comprises a wide clinical spectrum ranging from inconspicuous solitary soft tissue nodules to multiple disseminated tumors resulting in life-threatening complications. Familial IM follows an autosomal dominant mode of in...

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Detalles Bibliográficos
Autores principales: Hettmer, Simone, Dachy, Guillaume, Seitz, Guido, Agaimy, Abbas, Duncan, Catriona, Jongmans, Marjolijn, Hirsch, Steffen, Kventsel, Iris, Kordes, Uwe, de Krijger, Ronald R., Metzler, Markus, Michaeli, Orli, Nemes, Karolina, Poluha, Anna, Ripperger, Tim, Russo, Alexandra, Smetsers, Stephanie, Sparber-Sauer, Monika, Stutz, Eveline, Bourdeaut, Franck, Kratz, Christian P., Demoulin, Jean-Baptiste
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484085/
https://www.ncbi.nlm.nih.gov/pubmed/32888134
http://dx.doi.org/10.1007/s10689-020-00204-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484085/
https://www.ncbi.nlm.nih.gov/pubmed/32888134
http://dx.doi.org/10.1007/s10689-020-00204-2

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