Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1897-4287
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation ; volume:18 ; number:1 ; day:16 ; month:11 ; year:2020 ; pages:1-6 ; date:12.2020
Hereditary cancer in clinical practice ; 18, Heft 1 (16.11.2020), 1-6, 12.2020
- Creator
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Khaddour, Karam
Fields, Ryan C.
Ansstas, Michael
Rosman, Ilana S.
Ansstas, George
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13053-020-00155-w
- URN
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urn:nbn:de:101:1-2020122719455767273461
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Khaddour, Karam
- Fields, Ryan C.
- Ansstas, Michael
- Rosman, Ilana S.
- Ansstas, George
- SpringerLink (Online service)
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MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years
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Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome
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A predictive model of metachronous colorectal cancer occurrence in Lynch syndrome
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome
A novel germline mutation in hMLH1 in three Korean women with endometrial cancer in a family of Lynch syndrome: case report and literature review
Endometrioid endometrial cancer “recurring” as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?