Neoplasia (Inherited)

Mucocutaneous neuromas: an underrecognized manifestation of PTEN hamartoma-tumor syndrome.
[16702501] Arch Dermatol 142(5): 625-32 (2006)

Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome.
[10522671] Arch Dermatol 135(10): 1227-35 (1999)

Cowden disease or multiple hamartoma syndrome--cutaneous clue to internal malignancy.
[12370126] Eur J Dermatol 12(5): 411-21 (2002)

Extracolonic manifestations of hereditary colorectal cancer syndromes.
[20011437] Clin Colon Rectal Surg 21(4): 263-72 (2008)

The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency.
[18366737] BMC Med Genet 9(-): 20 (2008)

BRCA1/2 associated hereditary breast cancer.
[18257128] J Zhejiang Univ Sci B 9(2): 85-9 (2008)

Multiple primary carcinomas of the colon and associated extracolonic primary malignant tumors.
[7065754] Ann Surg 195(4): 501-7 (1982)

Selected aspects of inherited susceptibility to prostate cancer and tumours of different site of origin.
[19725994] Hered Cancer Clin Pract 5(3): 164-79 (2007)

Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee.
[9818066] Ann Oncol 9(9): 939-50 (1998)

Hereditary cancer: ascertainment and management.
[36967] CA Cancer J Clin 29(4): 216-32 (1979)

Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management, and controversies.
[18798544] Cancer 113(7 Suppl): 1807-43 (2008)

Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy.
[18442100] Cancer 112(12): 2655-63 (2008)

Chemoprevention in hereditary colorectal cancer syndromes.
[10630181] Cancer 86(11 Suppl): 2551-63 (1999)

Genetic testing and counseling for hereditary forms of colorectal cancer.
[10630180] Cancer 86(11 Suppl): 2540-50 (1999)

Clinical challenges in management of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.
[10630179] Cancer 86(11 Suppl): 2533-9 (1999)

Managing hereditary ovarian cancer risk.
[10630177] Cancer 86(11 Suppl): 2517-24 (1999)

Prophylactic mastectomy and inherited predisposition to breast carcinoma.
[10630176] Cancer 86(11 Suppl): 2502-16 (1999)

Inherited genetic predisposition in breast cancer. A population-based perspective.
[10630175] Cancer 86(11 Suppl): 2493-501 (1999)

Genetic cancer risk assessment. Putting it all together.
[10630174] Cancer 86(11 Suppl): 2483-92 (1999)

Von Hippel-Lindau syndrome. A pleomorphic condition.
[10630173] Cancer 86(11 Suppl): 2478-82 (1999)

The genetics of hereditary melanoma and nevi. 1998 update.
[10630172] Cancer 86(11 Suppl): 2464-77 (1999)

New issues in genetic counseling of hereditary colon cancer.
[18006790] Clin Cancer Res 13(22 Pt 2): 6857s-61s (2007)

Recognition and management of hereditary breast cancer syndromes.
[14755011] Oncologist 9(1): 13-24 (2004)

Genetics of cancer predisposition.
[2889524] Cancer Res 47(21): 5518-27 (1987)

Why have we failed to find the low penetrance genetic constituents of common cancers?
[12496041] Cancer Epidemiol Biomarkers Prev 11(12): 1544-9 (2002)

Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model.
[19654196] CMAJ 181(5): 273-80 (2009)

Cancer surveillance based on imaging techniques in carriers of BRCA1/2 gene mutations: a systematic review.
[18208856] Br J Radiol 81(963): 172-9 (2008)

Hereditary cancer: guidelines in clinical practice--general overview.
[15477294] Ann Oncol 15 Suppl 4(-): iv121-5 (2004)

Hereditary cancer: guidelines in clinical practice. Colorectal cancer genetics.
[15477295] Ann Oncol 15 Suppl 4(-): iv127-31 (2004)

Hereditary cancer: guidelines in clinical practice. Breast and ovarian cancer genetics.
[15477297] Ann Oncol 15 Suppl 4(-): iv133-8 (2004)

Genetic counselling for hereditary predisposition to ovarian and breast cancer.
[20943638] Ann Oncol 21 Suppl 7(-): vii334-8 (2010)

Familial colorectal cancer risk: ESMO clinical recommendations.
[19454462] Ann Oncol 20 Suppl 4(-): 51-3 (2009)

Carney triad: a syndrome featuring paraganglionic, adrenocortical, and possibly other endocrine tumors.
[19723753] J Clin Endocrinol Metab 94(10): 3656-62 (2009)

Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency.
[21880633] Haematologica 96(12): 1892-4 (2011)

Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation.
[20015892] Haematologica 95(5): 841-4 (2010)

Constitutional mismatch repair-deficiency syndrome.
[20442441] Haematologica 95(5): 699-701 (2010)

Hereditary myeloproliferative disorders.
[20065077] Haematologica 95(1): 6-8 (2010)

Genetic susceptibility to lymphoma.
[17606447] Haematologica 92(7): 960-9 (2007)

BRCA and beyond: A genome-first approach to familial breast cancer risk assessment.
[22127114] Discov Med 12(66): 433-43 (2011)

The inherited genetics of ovarian and endometrial cancer.
[20456938] Curr Opin Genet Dev 20(3): 231-8 (2010)

Candidate gene association studies: successes and failures.
[20417090] Curr Opin Genet Dev 20(3): 257-61 (2010)

Advances in the genetics of familial renal cancer.
[20484339] Oncologist 15(6): 532-8 (2010)

Genetic aspects of familial thyroid cancer.
[19465682] Oncologist 14(6): 571-7 (2009)

Hereditary kidney cancer: unique opportunity for disease-based therapy.
[19402075] Cancer 115(10 Suppl): 2252-61 (2009)

An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.
[20208042] Am J Respir Crit Care Med 181(6): 626-44 (2010)

Susceptibility pathways in Fanconi's anemia and breast cancer.
[20484397] N Engl J Med 362(20): 1909-19 (2010)

Hereditary colorectal cancer.
[12621137] N Engl J Med 348(10): 919-32 (2003)

Hereditary breast and ovarian cancer: new genes, new treatments, new concepts.
[21637635] Dtsch Arztebl Int 108(19): 323-30 (2011)

Inherited forms of renal cell carcinoma.
[15285561] Scand J Surg 93(2): 103-11 (2004)

Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information.
[19319160] Eur J Hum Genet 17(7): 872-80 (2009)

Hereditary and familial colon cancer.
[20420945] Gastroenterology 138(6): 2044-58 (2010)

A knockout for Lynch syndrome.
[20102757] Gastroenterology 138(3): 820-2 (2010)

Cancer genetics: risks and mechanisms of cancer in women with inherited susceptibility to epithelial ovarian cancer.
[20811826] Cancer Treat Res 156(-): 69-85 (2010)

Familial chronic lymphocytic leukemia.
[20389242] Curr Opin Hematol 17(4): 350-5 (2010)

Identifying and testing for hereditary susceptibility to common cancers.
[15537575] CA Cancer J Clin 54(6): 309-26 (2004)

Educational paper: screening in cancer predisposition syndromes: guidelines for the general pediatrician.
[21210147] Eur J Pediatr 170(3): 285-94 (2011)

Lessons learned from DNA repair defective syndromes.
[17518994] Exp Dermatol 16(6): 532-44 (2007)

Hereditary diffuse gastric cancer: prophylactic surgical oncology implications.
[18672140] Surg Clin North Am 88(4): 759-78, vi-vii (2008)

Hamartomatous polyposis syndromes.
[18672141] Surg Clin North Am 88(4): 779-817, vii (2008)

Family cancer syndromes: inherited deficiencies in systems for the maintenance of genomic integrity.
[19056039] Surg Oncol Clin N Am 18(1): 1-17, vii (2009)

Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany.
[22109790] J Community Genet 2(2): 53-69 (2011)

Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
[20587412] J Med Genet 47(9): 579-85 (2010)

Genetics of skin appendage neoplasms and related syndromes.
[16272260] J Med Genet 42(11): 811-9 (2005)

Mechanisms of inherited cancer susceptibility.
[18196605] J Zhejiang Univ Sci B 9(1): 1-4 (2008)

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives.
[19125126] Genet Med 11(1): 35-41 (2009)

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
[19125127] Genet Med 11(1): 42-65 (2009)

Mendelian genetics of rare--and not so rare--cancers.
[20946573] Ann N Y Acad Sci 1214(): 70-82 (2010)

Mouse models of inherited cancer syndromes.
[21075289] Hematol Oncol Clin North Am 24(6): 1205-28 (2010)

Rare and unusual endocrine cancer syndromes with mutated genes.
[21167385] Semin Oncol 37(6): 680-90 (2010)

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