Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group

Lea Guerrini-Rousseau, Julien Masliah-Planchon, Sebastian M. Waszak, Pia Alhopuro, Patrick R. Benusiglio, Franck Bourdeaut, Ines B. Brecht, Giada Del Baldo, Sandeep Kumar Dhanda, Maria Luisa Garre, Corrie E. M. Gidding, Steffen Hirsch, Pauline Hoarau, Mette Jorgensen, Christian Kratz, Lucie Lafay-Cousin, Angela Mastronuzzi, Lorenza Pastorino, Stefan M. Pfister, Christopher SchroederMiriam Jane Smith, Pia Vahteristo, Roseline Vibert, Catheline Vilain, Nicolas Waespe, Ingrid M. Winship, D. Gareth Evans, Laurence Brugieres

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalJournal of Medical Genetics
Volume59
Issue number11
Pages (from-to)1123-1132
Number of pages10
ISSN0022-2593
DOIs
Publication statusPublished - Nov 2022
MoE publication typeA1 Journal article-refereed

Fields of Science

  • genetic predisposition to disease
  • germ-line mutation
  • central nervous system diseases
  • genetic counseling
  • congenital
  • hereditary
  • and neonatal diseases and abnormalities
  • CHILDHOOD MEDULLOBLASTOMA
  • GORLIN SYNDROME
  • HUMAN HOMOLOG
  • MUTATIONS
  • PREDISPOSITION
  • CHILDREN
  • FAMILY
  • GENE
  • 3111 Biomedicine
  • 1184 Genetics, developmental biology, physiology

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