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The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations

Journal of medical genetics, 2004-07, Vol.41 (7), p.484-491

2004

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Prevention and management of duodenal polyps in familial adenomatous polyposis

Gut, 2005-07, Vol.54 (7), p.1034-1043

2005

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Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis

Gut, 2008-05, Vol.57 (5), p.623-627

2008

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Colorectal cancer screening: Clinical guidelines and rationale

Gastroenterology (New York, N.Y. 1943), 1997-02, Vol.112 (2), p.594-642

1997

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Sulindac targets nuclear β-catenin accumulation and Wnt signalling in adenomas of patients with familial adenomatous polyposis and in human colorectal cancer cell lines

British journal of cancer, 2004-01, Vol.90 (1), p.224-229

2004

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The Use and Interpretation of Commercial APC Gene Testing for Familial Adenomatous Polyposis

The New England journal of medicine, 1997-03, Vol.336 (12), p.823-827

1997

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Oral and maxillofacial manifestations of familial adenomatous polyposis

Oral diseases, 2007-07, Vol.13 (4), p.360-365

2007

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AGA technical review on hereditary colorectal cancer and genetic testing

Gastroenterology (New York, N.Y. 1943), 2001-07, Vol.121 (1), p.198-213

2001

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Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis

Gut, 2006-01, Vol.55 (1), p.1-5

2006

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Screening and Surveillance for the Early Detection of Colorectal Cancer and Adenomatous Polyps, 2008: A Joint Guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology

CA: a cancer journal for clinicians, 2008-05, Vol.58 (3), p.130-160

2008

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Phenotypic and molecular characteristics of hyperplastic polyposis

Gastroenterology (New York, N.Y. 1943), 2000-08, Vol.119 (2), p.323-332

2000

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Mucosal prolapse syndrome presenting as rectal polyposis

Journal of clinical pathology, 2009-11, Vol.62 (11), p.1034-1036

2009

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

Nature genetics, 1997-09, Vol.17 (1), p.79-83

1997

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Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Clinical genetics, 2007-12, Vol.72 (6), p.568-573

2007

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Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis

Annals of surgical oncology, 2002-11, Vol.9 (9), p.901-906

2002

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Risk of colorectal cancer in juvenile polyposis

Gut, 2007-07, Vol.56 (7), p.965-967

2007

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Collagenous colitis with mucosal tears on endoscopic insufflation: a unique presentation

Gut, 2002-10, Vol.51 (4), p.600-600

2002

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Hepatoblastoma and APC gene mutation in familial adenomatous polyposis

Gut, 1996-12, Vol.39 (6), p.867-869

1996

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Treatment of Colonic and Rectal Adenomas with Sulindac in Familial Adenomatous Polyposis

The New England journal of medicine, 1993-05, Vol.328 (18), p.1313-1316

1993

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Inhibition of apoptosis during development of colorectal cancer

Cancer research (Chicago, Ill.), 1995-05, Vol.55 (9), p.1811-1816

1995

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Peutz-Jeghers Syndrome and Management Recommendations

Clinical gastroenterology and hepatology, 2006-04, Vol.4 (4), p.408-415

2006

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Molecular Diagnosis of Familial Adenomatous Polyposis

The New England journal of medicine, 1993-12, Vol.329 (27), p.1982-1987

1993

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Increased risk of thyroid and pancreatic carcinoma in familial adenomatous polyposis

Gut, 1993-10, Vol.34 (10), p.1394-1396

1993

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Loss of IGF2 Imprinting: A Potential Marker of Colorectal Cancer Risk

Science (American Association for the Advancement of Science), 2003-03, Vol.299 (5613), p.1753-1755

2003

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Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene

Gut, 1998-10, Vol.43 (4), p.548-552

1998

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The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations

Prevention and management of duodenal polyps in familial adenomatous polyposis

Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis

Colorectal cancer screening: Clinical guidelines and rationale

Sulindac targets nuclear β-catenin accumulation and Wnt signalling in adenomas of patients with familial adenomatous polyposis and in human colorectal cancer cell lines

The Use and Interpretation of Commercial APC Gene Testing for Familial Adenomatous Polyposis

Oral and maxillofacial manifestations of familial adenomatous polyposis

AGA technical review on hereditary colorectal cancer and genetic testing

Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis

Screening and Surveillance for the Early Detection of Colorectal Cancer and Adenomatous Polyps, 2008: A Joint Guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology

Phenotypic and molecular characteristics of hyperplastic polyposis

Mucosal prolapse syndrome presenting as rectal polyposis

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis

Risk of colorectal cancer in juvenile polyposis

Collagenous colitis with mucosal tears on endoscopic insufflation: a unique presentation

Hepatoblastoma and APC gene mutation in familial adenomatous polyposis

Treatment of Colonic and Rectal Adenomas with Sulindac in Familial Adenomatous Polyposis

Inhibition of apoptosis during development of colorectal cancer

Peutz-Jeghers Syndrome and Management Recommendations

Molecular Diagnosis of Familial Adenomatous Polyposis

Increased risk of thyroid and pancreatic carcinoma in familial adenomatous polyposis

Loss of IGF2 Imprinting: A Potential Marker of Colorectal Cancer Risk

Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene

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