STK11 genotyping and cancer risk in Peutz-Jeghers syndrome

Journal of Medical Genetics

Volumn 42, Issue 5, 2005, Pages 428-435

  Schumacher, Volérie ^a   Vogel, T ^a   Leube, B ^a   Driemel, C ^a   Goecke, T ^a   Moslein G ^a   Royer Pokora, B ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE;

ARTICLE; CANCER CLASSIFICATION; CANCER RISK; CANCER SCREENING; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; GENE; GENE DELETION; GENE MUTATION; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEUTZ JEGHERS SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING; SINGLE STRAND CONFORMATION POLYMORPHISM; STK11 GENE;

ADOLESCENT; ADULT; AGED; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HUMANS; MIDDLE AGED; MUTATION; NEOPLASMS; PEUTZ-JEGHERS SYNDROME; PROTEIN-SERINE-THREONINE KINASES;

EID: 18844439886     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2004.026294     Document Type: Article

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