A novel mutation in STK11gene is associated with Peutz-Jeghers Syndrome in Indian patients
- 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 STK11gene is associated with Peutz-Jeghers Syndrome in Indian patients ; volume:7 ; number:1 ; day:30 ; month:9 ; year:2006 ; pages:1-6 ; date:12.2006
BMC medical genetics ; 7, Heft 1 (30.9.2006), 1-6, 12.2006
- Creator
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Thakur, Nikita
- Contributor
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Reddy, D Nageshwar
Rao, G Venkat
Mohankrishna, P.
Singh, Lalji
Chandak, Giriraj R.
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-7-73
- URN
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urn:nbn:de:1111-2016021833001
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:22 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Thakur, Nikita
- Reddy, D Nageshwar
- Rao, G Venkat
- Mohankrishna, P.
- Singh, Lalji
- Chandak, Giriraj R.
- SpringerLink (Online service)
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Peutz–Jeghers syndrome in capsule endoscopy and balloon enteroscopy
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Bladder hamartoma in Peutz-Jeghers syndrome: a rare case report
A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients
A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report
A novel missense mutation of the STK11 gene in a Chinese family with Peutz-Jeghers syndrome
High prevalence of germline STK11mutations in Hungarian Peutz-Jeghers Syndrome patients