A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- 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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A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report ; volume:18 ; number:1 ; day:23 ; month:2 ; year:2017 ; pages:1-6 ; date:12.2017
BMC medical genetics ; 18, Heft 1 (23.2.2017), 1-6, 12.2017
- Creator
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Chen, Jing-Hui
- Contributor
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Zheng, Jing-Jing
Guo, Qin
Liu, Chao
Luo, Bin
Tang, Shuang-Bo
Cheng, Jian-Ding
Huang, Er-Wen
SpringerLink (Online service)
- DOI
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10.1186/s12881-017-0373-z
- URN
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urn:nbn:de:1111-2017031618979
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:01 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Chen, Jing-Hui
- Zheng, Jing-Jing
- Guo, Qin
- Liu, Chao
- Luo, Bin
- Tang, Shuang-Bo
- Cheng, Jian-Ding
- Huang, Er-Wen
- SpringerLink (Online service)
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Diagnostic difficulty in Peutz–Jeghers syndrome
Fractal approach to the fluidity of a cement mortar
Beitrag zum Lokalisationsproblem beim Peutz-Jeghers-Syndrom
Besondere klinische Verlaufsform einer Peutz-Jeghers-Hamartie
Untersuchungen zur formalen Pathogenese des Peutz-Jeghers-Polypen
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A novel mutation in STK11gene is associated with Peutz-Jeghers Syndrome in Indian patients
Kasuistischer Beitrag zum Peutz-Touraine-Jeghers-Syndrom im Kindesalter
Genetic variation at a splicing branch point in intron 7 of STK11: a rare variant decreasing its expression in a Chinese family with Peutz–Jeghers syndrome
Nosologische Studien zum Peutz-Jeghers-Syndrom
Panendoscopic characterization of Peutz–Jeghers syndrome
Diagnostic difficulty in Peutz–Jeghers syndrome
Fractal approach to the fluidity of a cement mortar
Beitrag zum Lokalisationsproblem beim Peutz-Jeghers-Syndrom
Besondere klinische Verlaufsform einer Peutz-Jeghers-Hamartie
Untersuchungen zur formalen Pathogenese des Peutz-Jeghers-Polypen
Melaena with Peutz-Jeghers syndrome: a case report
Mutations in STK11gene in Czech Peutz-Jeghers patients
A novel mutation in STK11gene is associated with Peutz-Jeghers Syndrome in Indian patients