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2. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature. Nieuwenhuis MH, Vasen HF. Crit Rev Oncol Hematol; 2007 Feb; 61(2):153-61. PubMed ID: 17064931 [Abstract] [Full Text] [Related]
3. Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC): a review of clinical, genetic and therapeutic aspects. Soravia C, Bapat B, Cohen Z. Schweiz Med Wochenschr; 1997 Apr 19; 127(16):682-90. PubMed ID: 9140167 [Abstract] [Full Text] [Related]
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6. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis. Bertario L, Russo A, Sala P, Varesco L, Giarola M, Mondini P, Pierotti M, Spinelli P, Radice P, Hereditary Colorectal Tumor Registry. J Clin Oncol; 2003 May 01; 21(9):1698-707. PubMed ID: 12721244 [Abstract] [Full Text] [Related]
7. Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindred. Scott RJ, Taeschner W, Heinimann K, Müller H, Dobbie Z, Morgenthaler S, Hoffmann F, Peterli B, Meyer UA. Eur J Hum Genet; 1997 May 01; 5(1):43-9. PubMed ID: 9156320 [Abstract] [Full Text] [Related]
8. Mutational screening of the APC gene in Chilean families with familial adenomatous polyposis: nine novel truncating mutations. De la Fuente MK, Alvarez KP, Letelier AJ, Bellolio F, Acuña ML, León FS, Pinto E, Carvallo P, López-Köstner F. Dis Colon Rectum; 2007 Dec 01; 50(12):2142-8. PubMed ID: 17963004 [Abstract] [Full Text] [Related]
9. Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations. Vandrovcová J, Stekrová J, Kebrdlová V, Kohoutová M. Hum Mutat; 2004 Apr 01; 23(4):397. PubMed ID: 15024739 [Abstract] [Full Text] [Related]
10. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome. Foulkes WD. QJM; 1995 Dec 01; 88(12):853-63. PubMed ID: 8593545 [Abstract] [Full Text] [Related]
12. [Hereditary colorectal cancer associated with polyposis syndromes]. Soravia C, Pocard M. Ann Chir; 1999 Nov 01; 53(10):979-84. PubMed ID: 10670145 [Abstract] [Full Text] [Related]
13. Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition. Wallis YL, Morton DG, McKeown CM, Macdonald F. J Med Genet; 1999 Jan 01; 36(1):14-20. PubMed ID: 9950360 [Abstract] [Full Text] [Related]
14. Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis. De Rosa M, Galatola M, Borriello S, Duraturo F, Masone S, Izzo P. Dis Colon Rectum; 2009 Feb 01; 52(2):268-74. PubMed ID: 19279422 [Abstract] [Full Text] [Related]
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16. Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristics. Bouguen G, Manfredi S, Blayau M, Dugast C, Buecher B, Bonneau D, Siproudhis L, David V, Bretagne JF. Dis Colon Rectum; 2007 Oct 01; 50(10):1612-7. PubMed ID: 17674103 [Abstract] [Full Text] [Related]
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18. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis. Parisi ML. J Am Optom Assoc; 1995 Feb 01; 66(2):106-12. PubMed ID: 7714311 [Abstract] [Full Text] [Related]
19. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred. Plasilova M, Russell AM, Wanner A, Wolf A, Dobbie Z, Müller HJ, Heinimann K. Eur J Hum Genet; 2004 May 01; 12(5):365-71. PubMed ID: 14735163 [Abstract] [Full Text] [Related]
20. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Yen T, Stanich PP, Axell L, Patel SG. ; 1993 May 01. PubMed ID: 20301519 [Abstract] [Full Text] [Related] Page: [Next] [New Search]