W. Lim

发表

Mapping of a translocation breakpoint in a Peutz–Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11‐negative PJS cases

R. Houlston, J. Shipley, I. Moore, 2004, Genes, chromosomes & cancer.

Further observations on LKB1/STK11 status and cancer risk in Peutz–Jeghers syndrome

R. Houlston, D. Eccles, I. Tomlinson, 2003, British Journal of Cancer.

Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

S. Gruber, R. Scott, R. Houlston, 2006, Clinical Cancer Research.

Relative frequency and morphology of cancers in STK11 mutation carriers.

S. Gruber, R. Scott, R. Houlston, 2004, Gastroenterology.

Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

R. Houlston, S. Hodgson, P. Morrison, 2005, Journal of Medical Genetics.

Exonic STK 11 deletions are not a rare cause of Peutz-Jeghers syndrome

R. Houlston, S. Hodgson, P. Morrison, 2006 .

Analysis of the CTLA4 Gene in Swedish Coeliac Disease Patients

S. Popat, R. Houlston, S. Bevan, 2002, Scandinavian journal of gastroenterology.

Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome

R. Houlston, I. Tomlinson, R. Trembath, 2005, BMC Genomics.

STK11 status and intussusception risk in Peutz-Jeghers syndrome

S. Gruber, R. Scott, R. Houlston, 2006, Journal of Medical Genetics.