Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.
暂无分享,去创建一个
[1] J. Toro,et al. Hereditary Leiomyomatosis and Renal Cell Cancer , 2020, Handbook of Tumor Syndromes.
[2] S. Sasidharanpillai,et al. Muir-Torre syndrome , 2020, Definitions.
[3] R. Scott,et al. Dupuytren’s disease and the risk of malignant neoplasms , 2014, Hereditary cancer in clinical practice.
[4] D. Mehregan,et al. Cowden syndrome: report of two cases with immunohistochemical analysis for PTEN expression. , 2012, The American Journal of dermatopathology.
[5] C. Zouboulis,et al. New pharmaceutical concepts for sebaceous gland diseases: implementing today's pre-clinical data into tomorrow's daily clinical practice. , 2012, Current pharmaceutical biotechnology.
[6] L. Aaltonen,et al. Strong family history of uterine leiomyomatosis warrants fumarate hydratase mutation screening. , 2012, Human reproduction.
[7] A. Fernandez-Flores. Considerations on the Performance of Immunohistochemistry for Mismatch Repair Gene Proteins in Cases of Sebaceous Neoplasms and Keratoacanthomas With Reference to Muir–Torre Syndrome , 2012, The American Journal of dermatopathology.
[8] C. Longo,et al. Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome , 2012, Familial Cancer.
[9] J. Mulliken,et al. PTEN Hamartoma of Soft Tissue: A Distinctive Lesion in PTEN Syndromes , 2012, The American journal of surgical pathology.
[10] A. Lazar,et al. Trichilemmomas show loss of PTEN in Cowden syndrome but only rarely in sporadic tumors , 2012, Journal of cutaneous pathology.
[11] Ming Zhou,et al. Papillary renal cell carcinoma is associated with PTEN hamartoma tumor syndrome. , 2012, Urology.
[12] Y. Yatabe,et al. Pulmonary Cysts of Birt-Hogg-Dubé Syndrome: A Clinicopathologic and Immunohistochemical Study of 9 Families , 2012, The American journal of surgical pathology.
[13] S. Seidenari,et al. Brooke‐Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor‐suppressor genes , 2012, Journal of cutaneous pathology.
[14] D. Evans,et al. Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes , 2012, Acta Neuropathologica.
[15] M. Kasper,et al. Basal cell carcinoma - molecular biology and potential new therapies. , 2012, The Journal of clinical investigation.
[16] C. Eng,et al. Lifetime Cancer Risks in Individuals with Germline PTEN Mutations , 2012, Clinical Cancer Research.
[17] P. Pontisso,et al. APCI1307K Mutations and Forkhead Box Gene (FOXO1A): Another Piece of an Interesting Correlation , 2012, The International journal of biological markers.
[18] E. Bongers,et al. Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families , 2011, British Journal of Cancer.
[19] Poonam K Sharma,et al. Renal medullary carcinomas: histopathologic phenotype associated with diverse genotypes. , 2011, Human pathology.
[20] D. Cooper,et al. Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis , 2011, Human Genomics.
[21] A. Bellizzi,et al. Immunohistochemical Staining of Thyroidectomy Specimens for PTEN Can Aid in the Identification of Patients With Cowden Syndrome , 2011, The American journal of surgical pathology.
[22] C. Eng,et al. Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations. , 2011, The Journal of clinical endocrinology and metabolism.
[23] P. Maxwell. Seeing the smoking gun: a sensitive and specific method to visualize loss of the tumour suppressor, fumarate hydratase, in human tissues , 2011, The Journal of pathology.
[24] A. Bree,et al. Consensus statement from the first international colloquium on basal cell nevus syndrome (BCNS) , 2011, American journal of medical genetics. Part A.
[25] L. Aaltonen,et al. Aberrant succination of proteins in fumarate hydratase‐deficient mice and HLRCC patients is a robust biomarker of mutation status , 2011, The Journal of pathology.
[26] S. Seidenari,et al. Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas , 2011, Hereditary cancer in clinical practice.
[27] E. Imyanitov,et al. Drug therapy for hereditary cancers , 2011, Hereditary cancer in clinical practice.
[28] M. Goetz,et al. Colonic polyposis and neoplasia in Cowden syndrome. , 2011, Mayo Clinic proceedings.
[29] G. Singh,et al. Post-translational modifications of PTEN and their potential therapeutic implications. , 2011, Current cancer drug targets.
[30] A. Rütten,et al. Multiple (Familial) Trichoepitheliomas: A Clinicopathological and Molecular Biological Study, Including CYLD and PTCH Gene Analysis, of a Series of 16 Patients , 2011, The American Journal of dermatopathology.
[31] E. Marqusee,et al. Thyroid nodules and cancer in children with PTEN hamartoma tumor syndrome. , 2011, The Journal of clinical endocrinology and metabolism.
[32] R. Benamouzig,et al. Endoscopic findings in Cowden syndrome. , 2011, Endoscopy.
[33] H. Lehtonen,et al. Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics , 2011, Familial Cancer.
[34] L. Thomas,et al. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma , 2011, Journal of Medical Genetics.
[35] Salma K. Marani,et al. Attitudes towards colorectal cancer screening in Lynch syndrome families: how do they change from pre-test genetic counseling to 6 and 12-months post-disclosure? , 2011, Hereditary Cancer in Clinical Practice.
[36] J. Lasota,et al. Succinate Dehydrogenase Subunit B (SDHB) Is Expressed in Neurofibromatosis 1-Associated Gastrointestinal Stromal Tumors (Gists): Implications for the SDHB Expression Based Classification of Gists , 2011, Journal of Cancer.
[37] J. Tille,et al. Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity. , 2011, Thyroid : official journal of the American Thyroid Association.
[38] L. Hoefsloot,et al. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis , 2011, Clinical genetics.
[39] C. Eng,et al. Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers. , 2010, Gastroenterology.
[40] J. Lehmann-Che,et al. Hereditary renal cancer syndromes: an update of a systematic review. , 2010, European urology.
[41] A. V. D. van den Ouweland,et al. Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis , 2010, Familial Cancer.
[42] P. Driggers,et al. Novel, orally active selective progesterone receptor modulator CP8947 inhibits leiomyoma cell proliferation without adversely affecting endometrium or myometrium , 2010, The Journal of Steroid Biochemistry and Molecular Biology.
[43] Andrew Shenton,et al. Basal Cell Carcinomas in Gorlin Syndrome: A Review of 202 Patients , 2010, Journal of skin cancer.
[44] W. Weyers,et al. Brooke-Spiegler Syndrome: Report of 10 Patients From 8 Families With Novel Germline Mutations: Evidence of Diverse Somatic Mutations in the Same Patient Regardless of Tumor Type , 2010, Diagnostic molecular pathology : the American journal of surgical pathology, part B.
[45] Jean Kanitakis. Adnexal tumours of the skin as markers of cancer‐prone syndromes , 2010, Journal of the European Academy of Dermatology and Venereology : JEADV.
[46] C. Yeo,et al. Periampullary and Duodenal Neoplasms in Neurofibromatosis Type 1: Two Cases and an Updated 20-Year Review of the Literature Yielding 76 Cases , 2010, Journal of Gastrointestinal Surgery.
[47] Maria Laura De Marchis,et al. Association between Birt Hogg Dube syndrome and cancer predisposition. , 2010, Anticancer research.
[48] T. Vaněček,et al. Brooke‐Spiegler syndrome: report of a case with a novel mutation in the CYLD gene and different types of somatic mutations in benign and malignant tumors , 2010, Journal of cutaneous pathology.
[49] A. Enk,et al. Entdeckung einer neuen Mutation im CYLD‐Gen bei einer Familie mit Brooke‐Spiegler‐Syndrom , 2010 .
[50] A. Lazar,et al. Sebaceous neoplasia and the Muir–Torre syndrome: important connections with clinical implications , 2010, Histopathology.
[51] M. Skrzypczak,et al. Multiple trichoepitheliomas – a novel mutation in the CYLD gene , 2009, Journal of the European Academy of Dermatology and Venereology : JEADV.
[52] J. Frank,et al. Clinical and molecular genetic aspects of hereditary multiple cutaneous leiomyomatosis. , 2009, European journal of dermatology : EJD.
[53] T. Vaněček,et al. A Case of Brooke-Spiegler Syndrome With a Novel Germline Deep Intronic Mutation in the CYLD Gene Leading to Intronic Exonization, Diverse Somatic Mutations, and Unusual Histology , 2009, The American Journal of dermatopathology.
[54] T. Vaněček,et al. Skin type spiradenoma of the parotid gland with malignant transformation: report of a case with analysis of the CYLD gene. , 2009, Human pathology.
[55] J. Toro,et al. Update of cylindromatosis gene (CYLD) mutations in Brooke‐Spiegler syndrome: novel insights into the role of deubiquitination in cell signaling , 2009, Human mutation.
[56] F. D. de Sauvage,et al. Mechanisms of Hedgehog pathway activation in cancer and implications for therapy. , 2009, Trends in pharmacological sciences.
[57] A. Rütten,et al. Morphologic Diversity of Malignant Neoplasms Arising in Preexisting Spiradenoma, Cylindroma, and Spiradenocylindroma Based on the Study of 24 Cases, Sporadic or Occurring in the Setting of Brooke-Spiegler Syndrome , 2009, The American journal of surgical pathology.
[58] A. Zauber,et al. Five-Year Efficacy and Safety Analysis of the Adenoma Prevention with Celecoxib Trial , 2009, Cancer Prevention Research.
[59] A. Guimarães,et al. PTCH1 isoforms in odontogenic keratocysts. , 2009, Oral oncology.
[60] R. Pilarski. Cowden Syndrome: A Critical Review of the Clinical Literature , 2009, Journal of Genetic Counseling.
[61] W. Linehan,et al. Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer. , 2008, Archives of dermatology.
[62] J. Frank,et al. Brooke–Spiegler syndrome complicated by unilateral hearing loss , 2008, International journal of dermatology.
[63] P. Dennis,et al. PTEN hamartoma tumor syndromes , 2008, European Journal of Human Genetics.
[64] A. Lazar,et al. Site and Tumor Type Predicts DNA Mismatch Repair Status in Cutaneous Sebaceous Neoplasia , 2008, The American journal of surgical pathology.
[65] Stephen B Gruber,et al. Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer. , 2008, Cancer genetics and cytogenetics.
[66] S. Seidenari,et al. Wnt Pathway, Angiogenetic and Hormonal Markers in Sporadic and Familial Adenomatous Polyposis-associated Juvenile Nasopharyngeal Angiofibromas (JNA) , 2008, Applied immunohistochemistry & molecular morphology : AIMM.
[67] M. Mahalingam,et al. MSH-6: extending the reliability of immunohistochemistry as a screening tool in Muir–Torre syndrome , 2008, Modern Pathology.
[68] L. Horev,et al. CYLD mutations in familial skin appendage tumours , 2008, Journal of Medical Genetics.
[69] P. Møller,et al. Guidelines for the clinical management of familial adenomatous polyposis (FAP) , 2008, Gut.
[70] M. Merino,et al. The Morphologic Spectrum of Kidney Tumors in Hereditary Leiomyomatosis and Renal Cell Carcinoma (HLRCC) Syndrome , 2007, The American journal of surgical pathology.
[71] E. Lucci-Cordisco,et al. Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC , 2007, Clinical genetics.
[72] C. Longo,et al. BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-associated polyposis pedigrees. , 2007, The Journal of investigative dermatology.
[73] B. Scheithauer,et al. Low grade malignant peripheral nerve sheath tumor with smooth muscle differentiation , 2007, Acta Neuropathologica.
[74] Ignacio Blanco,et al. Conventional renal cancer in a patient with fumarate hydratase mutation. , 2007, Human pathology.
[75] M. Novelli,et al. An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation , 2007, Familial Cancer.
[76] Ximing J. Yang,et al. Birt-Hogg-Dubé syndrome: clinicopathologic findings and genetic alterations. , 2006, Archives of pathology & laboratory medicine.
[77] D. Evans,et al. Guidelines for the diagnosis and management of individuals with neurofibromatosis 1 , 2006, Journal of Medical Genetics.
[78] J. Hartley,et al. Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling , 2006, Proceedings of the National Academy of Sciences.
[79] S. Seidenari,et al. Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas. , 2006, The Journal of investigative dermatology.
[80] R. Szigeti,et al. CYLD mutations underlie Brooke–Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes , 2006, Clinical genetics.
[81] Eero Pukkala,et al. Analysis of fumarate hydratase mutations in a population‐based series of early onset uterine leiomyosarcoma patients , 2006, International journal of cancer.
[82] G Pellacani,et al. Attenuated familial adenomatous polyposis and Muir–Torre syndrome linked to compound biallelic constitutional MYH gene mutations , 2005, Clinical genetics.
[83] L. Aaltonen,et al. Increased risk of cancer in patients with fumarate hydratase germline mutation , 2005, Journal of Medical Genetics.
[84] P. Choyke,et al. Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer , 2005, Journal of Medical Genetics.
[85] S. Seidenari,et al. Different phenotypes in Muir–Torre syndrome: clinical and biomolecular characterization in two Italian families , 2005, The British journal of dermatology.
[86] M. Fukayama,et al. Gastrointestinal Stromal Tumors of Neurofibromatosis Type I (von Recklinghausen's Disease) , 2005, The American journal of surgical pathology.
[87] M. Gill,et al. Mutations in the CYLD gene in Brooke-Spiegler syndrome, familial cylindromatosis, and multiple familial trichoepithelioma: lack of genotype-phenotype correlation. , 2005, The Journal of investigative dermatology.
[88] R. Cusano,et al. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients , 2005, Human mutation.
[89] S. Seidenari,et al. Identification of Muir–Torre syndrome among patients with sebaceous tumors and keratoacanthomas , 2005, Cancer.
[90] A. Rowan,et al. Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndrome. , 2005, Archives of dermatology.
[91] C. Zouboulis. Acne and sebaceous gland function. , 2004, Clinics in dermatology.
[92] P. Propping,et al. A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome , 2004, Journal of Medical Genetics.
[93] L. Roncucci,et al. Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas. , 2004, Pathology, research and practice.
[94] P. Choyke,et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. , 2003, American journal of human genetics.
[95] W. Linehan,et al. Renal Tumors in the Birt-Hogg-Dubé Syndrome , 2002, The American journal of surgical pathology.
[96] Maria Merino,et al. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome. , 2002, Cancer cell.
[97] S. Velasco-Miguel,et al. Epidermal growth factor receptor signaling pathways are associated with tumorigenesis in the Nf1:p53 mouse tumor model. , 2002, Cancer research.
[98] D. Evans,et al. Malignant peripheral nerve sheath tumours in neurofibromatosis 1 , 2002, Journal of medical genetics.
[99] P. Choyke,et al. Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[100] A. Paetau,et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer , 2002, Nature Genetics.
[101] D. Gutmann,et al. International consensus statement on malignant peripheral nerve sheath tumors in neurofibromatosis. , 2002, Cancer research.
[102] C. Zouboulis,et al. Chronological ageing and photoageing of the human sebaceous gland , 2001, Clinical and experimental dermatology.
[103] N. Lindor,et al. Cutaneous sinus tract of dental origin , 2001, International journal of dermatology.
[104] J. Faivre,et al. Colorectal adenocarcinoma in patients under 45 years of age: Comparison with older patients in a well-defined french population , 2001, Diseases of the colon and rectum.
[105] L. Aaltonen,et al. Inherited susceptibility to uterine leiomyomas and renal cell cancer , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[106] I. Tomlinson,et al. Explaining differences in the severity of familial adenomatous polyposis and the search for modifier genes , 2001, Gut.
[107] A. King,et al. Malignant peripheral nerve sheath tumors in neurofibromatosis 1. , 2000, American journal of medical genetics.
[108] A. Ashworth,et al. Identification of the familial cylindromatosis tumour-suppressor gene , 2000, Nature Genetics.
[109] R. Gomez,et al. PTCH Gene Mutations in Odontogenic Keratocysts , 2000, Journal of dental research.
[110] M. Leppert,et al. The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect , 1999, Human Genetics.
[111] B. Korf,et al. Structural anomalies revealed by neuroimaging studies in the brains of patients with neurofibromatosis type 1 and large deletions , 1999, Genetics in Medicine.
[112] C. Has,et al. [Multiple cutaneous cylindromas associated with parotid and submandibular gland cylindromas]. , 1998, Annales de dermatologie et de venereologie.
[113] E. Telford,et al. Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndrome , 1997, Human Genetics.
[114] W. Bodmer,et al. Allele loss in colorectal cancer at the Cowden disease/juvenile polyposis locus on 10q. , 1997, Cancer genetics and cytogenetics.
[115] A. Goldstein,et al. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. , 1997, American journal of medical genetics.
[116] D. Cooper,et al. Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene , 1996, Human Genetics.
[117] M. Scott,et al. The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog , 1996, Nature.
[118] R. Myers,et al. Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome , 1996, Science.
[119] E. Mariman,et al. Localization of the gene for Cowden disease to chromosome 10q22–23 , 1996, Nature Genetics.
[120] M. Stratton,et al. Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12–q13: evidence for its role as a tumour suppressor gene , 1995, Nature Genetics.
[121] L. Roncucci,et al. Clinical and biologic features of adenomatosis coli in Northern Italy. , 1995, Scandinavian journal of gastroenterology.
[122] G. Thomas,et al. Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. , 1995, Human molecular genetics.
[123] R. Hennekam,et al. Dermal eccrine cylindromatosis. , 1994, Journal of medical genetics.
[124] P. Propping,et al. Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer , 1994, The Lancet.
[125] D. Evans,et al. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. , 1993, Journal of medical genetics.
[126] P. Borgen,et al. Cowden's disease. A case report with analyses at the molecular level , 1992, Cancer.
[127] H. Järvinen. Epidemiology of familial adenomatous polyposis in Finland: impact of family screening on the colorectal cancer rate and survival. , 1992, Gut.
[128] G. Williams,et al. Gastrointestinal manifestations of type 1 neurofibromatosis (von Recklinghausen's disease) , 1991, Histopathology.
[129] R. Martuza,et al. Benign spinal nerve sheath tumors: their occurrence sporadically and in neurofibromatosis types 1 and 2. , 1991, Journal of neurosurgery.
[130] D. Bardenstein,et al. Cowden's disease. , 1988, Ophthalmology.
[131] J. Cream,et al. (59) Case for diagnosis: possible Cowden's disease (multiple hamartoma and neoplasia syndrome) , 1988 .
[132] R. Browne,et al. The odontogenic keratocyst and its occurrence in the nevoid basal cell carcinoma syndrome. , 1987, Oral surgery, oral medicine, and oral pathology.
[133] F. Arwert,et al. The Cowden syndrome: a clinical and genetic study in 21 patients , 1986, Clinical genetics.
[134] H. Aram,et al. Multiple hamartoma syndrome (Cowden's disease) , 1983, Journal of the American Academy of Dermatology.
[135] B. Scheithauer,et al. 4 MALIGNANT PERIPHERAL NERVE SHEATH TUMORS WITH DIVERGENT DIFFERENTIATION , 1983 .
[136] W. Steck,et al. Cowden's disease (multiple hamartoma and neoplasia syndrome). A case report and review of the English literature. , 1983, Journal of the American Academy of Dermatology.
[137] H. Lindeberg,et al. [The nevoid basal cell carcinoma syndrome - Gorlin syndrome]. , 1980, Ugeskrift for laeger.
[138] W. J. Dubé,et al. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons. , 1977, Archives of dermatology.
[139] L. Celli,et al. [Gardner's syndrome]. , 1974, Minerva gastroenterologica.
[140] P. Weary,et al. Multiple hamartoma syndrome (Cowden's disease). , 1972, Archives of dermatology.
[141] D. Stevanović. Nevoid basal cell carcinoma syndrome. , 1967, Archives of dermatology.
[142] E. Muir,et al. Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato‐acanthomata of the face , 1967, The British journal of surgery.
[143] Richard G. Frank,et al. Archives of pathology , 1949 .
[144] K. J. Franklin.. Acta Chirurgica Scandinavica. , 1930 .
[145] S. West. Recurrent Pneumothorax , 1889 .
[146] R. Chamberlain,et al. Neoplasms associated with germline and somatic NF1 gene mutations. , 2012, The oncologist.
[147] A. Enk,et al. New mutation in the CYLD gene within a family with Brooke-Spiegler syndrome. , 2010, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.
[148] M. Leppert,et al. Erratum: The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect (Human Genetics (1999) 105 (388-398)) , 2000 .
[149] G. Chenevix-Trench,et al. Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. , 1997, American journal of human genetics.
[150] P. O'Connell,et al. Genomic organization of the neurofibromatosis 1 gene (NF1). , 1995, Genomics.
[151] M. Anti,et al. Cowden's disease with extensive gastrointestinal polyposis. , 1994, Journal of clinical gastroenterology.
[152] M. P. Leòn,et al. Hereditary gastrointestinal polyposis syndromes. , 1994, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.
[153] Y. Nakamura,et al. The role of the adenomatous polyposis coli (APC) gene in human cancers. , 1993, Advances in cancer research.
[154] J. Woodruff,et al. Glandular peripheral nerve sheath tumors. , 1993, Cancer.
[155] B. Ponder,et al. Inherited predisposition to cancer. , 1990, Trends in genetics : TIG.
[156] S. Winawer,et al. Early identification of individuals at increased risk for cancer of the large intestine. Part I: definition of high risk populations. , 1981, Clinical bulletin.
[157] S. Winawer,et al. Early identification of individuals at increased risk for cancer of the large intestine. Part II: development of risk factor profiles. , 1981, Clinical bulletin.
[158] K. Ishak,et al. Benign tumors and pseudotumors of the gallbladder. Report of 180 cases. , 1970, Archives of pathology.
[159] M. Karno,et al. Renal cell carcinoma. , 1956, Bulletin. Tufts-New England Medical Center.