Your browser doesn't support javascript.
loading
High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
Papp, Janos; Kovacs, Marietta Eva; Solyom, Szilvia; Kasler, Miklos; Børresen-Dale, Anne-Lise; Olah, Edith.
Affiliation
  • Papp J; Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary.
BMC Med Genet ; 11: 169, 2010 Nov 30.
Article in En | MEDLINE | ID: mdl-21118512
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peutz-Jeghers Syndrome / Protein Serine-Threonine Kinases / Germ-Line Mutation / White People Type of study: Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Hungary Country of publication: United kingdom
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peutz-Jeghers Syndrome / Protein Serine-Threonine Kinases / Germ-Line Mutation / White People Type of study: Prevalence_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Hungary Country of publication: United kingdom