Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs

In clinical practice, there are a number of cancer patients with clear family histories, but the patients lack mutations in known familial cancer syndrome genes. Recent advances in genomic technologies have enhanced the possibility of identifying causative genes in such cases. Two siblings, an elder...

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Detalles Bibliográficos
Autores principales: Kukita, Yoji, Okami, Jiro, Yoneda-Kato, Noriko, Nakamae, Ikuko, Kawabata, Takeshi, Higashiyama, Masahiko, Kato, Junya, Kodama, Ken, Kato, Kikuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111006/
https://www.ncbi.nlm.nih.gov/pubmed/27900359
http://dx.doi.org/10.1101/mcs.a001032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111006/
https://www.ncbi.nlm.nih.gov/pubmed/27900359
http://dx.doi.org/10.1101/mcs.a001032

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