Germline multigene panel testing revealed a BRCA2 pathogenic variant in a patient with suspected Lynch syndrome

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2192-3183

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Germline multigene panel testing revealed a BRCA2 pathogenic variant in a patient with suspected Lynch syndrome ; day:9 ; month:10 ; year:2020 ; pages:1-5
International Cancer Conference journal ; (9.10.2020), 1-5

Creator: Yoshihama, Tomoko
Hirasawa, Akira
Sugano, Kokichi
Yoshida, Teruhiko
Ushiama, Mineko
Ueki, Arisa
Akahane, Tomoko
Nanki, Yoshiko
Sakai, Kensuke
Makabe, Takeshi
Yamagami, Wataru
Susumu, Nobuyuki
Kameyama, Kaori
Kosaki, Kenjiro
Aoki, Daisuke

Contributor: SpringerLink (Online service)

DOI: 10.1007/s13691-020-00449-9

URN: urn:nbn:de:101:1-2020112323493278058611

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:34 AM CEST

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Associated

Yoshihama, Tomoko
Hirasawa, Akira
Sugano, Kokichi
Yoshida, Teruhiko
Ushiama, Mineko
Ueki, Arisa
Akahane, Tomoko
Nanki, Yoshiko
Sakai, Kensuke
Makabe, Takeshi
Yamagami, Wataru
Susumu, Nobuyuki
Kameyama, Kaori
Kosaki, Kenjiro
Aoki, Daisuke
SpringerLink (Online service)

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Germline multigene panel testing revealed a BRCA2 pathogenic variant in a patient with suspected Lynch syndrome

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Other Objects (12)

The germline mutational landscape of BRCA1 and BRCA2 in Brazil

BRCA1 and BRCA2 germline mutation analysis in the Indonesian population

BRCA2 germline mutation carrier with five malignancies: a case report

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

BRCA1 and BRCA2 germline mutations in Chinese Hakka breast cancer patients

Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers

Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil

BRCA2 germline mutation in familial leukaemia with familial breast cancer: a case report

A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

The germline mutational landscape of BRCA1 and BRCA2 in Brazil

BRCA1 and BRCA2 germline mutation analysis in the Indonesian population

BRCA2 germline mutation carrier with five malignancies: a case report

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

BRCA1 and BRCA2 germline mutations in Chinese Hakka breast cancer patients

Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers

Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil

BRCA2 germline mutation in familial leukaemia with familial breast cancer: a case report

A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

The germline mutational landscape of BRCA1 and BRCA2 in Brazil

BRCA1 and BRCA2 germline mutation analysis in the Indonesian population

BRCA2 germline mutation carrier with five malignancies: a case report

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

BRCA1 and BRCA2 germline mutations in Chinese Hakka breast cancer patients

Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers

Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil

BRCA2 germline mutation in familial leukaemia with familial breast cancer: a case report

A case of strongly suspected Lynch syndrome with colorectal neuroendocrine carcinoma

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

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