- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Mutations in STK11gene in Czech Peutz-Jeghers patients ; volume:10 ; number:1 ; day:19 ; month:7 ; year:2009 ; pages:1-8 ; date:12.2009
BMC medical genetics ; 10, Heft 1 (19.7.2009), 1-8, 12.2009
- Creator
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Vasovčák, Peter
- Contributor
-
Puchmajerová, Alena
Roubalík, Jan
Křepelová, Anna
SpringerLink (Online service)
- DOI
-
10.1186/1471-2350-10-69
- URN
-
urn:nbn:de:1111-2016021835873
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vasovčák, Peter
- Puchmajerová, Alena
- Roubalík, Jan
- Křepelová, Anna
- SpringerLink (Online service)
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Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome
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Panendoscopic characterization of Peutz–Jeghers syndrome
Diagnostic difficulty in Peutz–Jeghers syndrome
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
High prevalence of germline STK11mutations in Hungarian Peutz-Jeghers Syndrome patients
Altered mucosal bacteria and metabolomics in patients with Peutz–Jeghers syndrome
A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome
Kasuistischer Beitrag zum Peutz-Touraine-Jeghers-Syndrom im Kindesalter
Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome
Nosologische Studien zum Peutz-Jeghers-Syndrom
Panendoscopic characterization of Peutz–Jeghers syndrome
Diagnostic difficulty in Peutz–Jeghers syndrome
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
High prevalence of germline STK11mutations in Hungarian Peutz-Jeghers Syndrome patients
Altered mucosal bacteria and metabolomics in patients with Peutz–Jeghers syndrome
A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome