STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients

Clinical Genetics

Volumn 56, Issue 2, 1999, Pages 136-141

  Jiang, Cao Yang ^c   Esufali, Susmita ^c   Berk, Terri ^c   Gallinger, Steven ^c   Cohen, Zane ^c   Tobi, Martin ^a   Redston, Mark ^c   Bapat, Bharati ^b  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b MOUNT SINAI HOSPITAL   (Canada)

^c NONE

Author keywords

Gastrointestinal hamartomas; Peutz Jeghers syndrome; Serine threonine kinase gene

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CANCER SUSCEPTIBILITY; CHROMOSOME 19P; CHROMOSOME MUTATION; CLINICAL ARTICLE; DNA SEQUENCE; EXON; FEMALE; GENE DELETION; GENE MAPPING; GENETIC POLYMORPHISM; GENOME; HAMARTOMA; HETEROZYGOSITY LOSS; HUMAN; INTESTINE POLYP; MALE; PEUTZ JEGHERS SYNDROME; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; GENE DELETION; GENETIC MARKERS; GERM-LINE MUTATION; HUMANS; INTRONS; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; PEDIGREE; PEUTZ-JEGHERS SYNDROME; PHENOTYPE; POLYMORPHISM, GENETIC; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 0032876595     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.560207.x     Document Type: Article

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