Simple and complex genetics of colorectal cancer susceptibilityBAGLIONI, Silvana; GENUARDI, Maurizio.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 35-43, issn 0148-7299, 9 p.Article

Genomic imprinting and environment in hereditary paragangliomaBAYSAL, Bora E.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 85-90, issn 0148-7299, 6 p.Article

Loss of DNA mismatch repair function and cancer predisposition in the mouse: Animal models for human hereditary nonpolyposis colorectal cancerEDELMANN, Lisa; EDELMANN, Winfried.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 91-99, issn 0148-7299, 9 p.Article

Unravelling the genetics of prostate cancerEDWARDS, Stephen M; EELES, Rosalind A.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 65-73, issn 0148-7299, 9 p.Article

Genetic conditions associated with intestinal juvenile polypsMERG, Anders; HOWE, James R.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 44-55, issn 0148-7299, 12 p.Article

Retinoblastoma: Revisiting the model prototype of inherited cancerLOHMANN, Dietmar R; GALLIE, Brenda L.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 23-28, issn 0148-7299, 6 p.Article

Familial Wilms tumorRUTESHOUSER, E. Cristy; HUFF, Vicki.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 29-34, issn 0148-7299, 6 p.Article

Breast cancer genetics: Unsolved questions and open perspectives in an expanding clinical practiceHODGSON, Shirley V; MORRISON, Patrick J; IRVING, Melita et al.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 56-64, issn 0148-7299, 9 p.Article

Genetic insights into familial tumors of the nervous systemMELEAN, German; SESTINI, Roberta; AMMANNATI, Franco et al.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 74-84, issn 0148-7299, 11 p.Article

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Inherited predisposition to cancer: A historical overviewLYNCH, Henry T; SHAW, Trudy G; LYNCH, Jane F et al.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 5-22, issn 0148-7299, 18 p.Article

Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific mannerTEDDE, Andrea; LAURA PUTIGNANO, Anna; BAGNOLI, Siro et al.Scandinavian journal of gastroenterology. 2008, Vol 43, Num 6, pp 712-718, issn 0036-5521, 7 p.Article

Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11)STAGI, Stefano; LAPI, Elisabetta; GAMBINERI, Eleonora et al.European journal of endocrinology. 2010, Vol 163, Num 2, pp 329-337, issn 0804-4643, 9 p.Article

Maternal-fetal flow, negative events, and preeclampsia: Role of ACE I/D polymorphismMELLO, Giorgio; PARRETTI, Elena; GENSINI, Francesca et al.Hypertension (Dallas, Tex. 1979). 2003, Vol 41, Num 4, pp 932-937, issn 0194-911X, 6 p.Article

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Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationBACCI, Costanza; SESTINI, Roberta; PROVENZANO, Aldesia et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 1, pp 73-80, issn 1364-6745, 8 p.Article

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Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation. CommentaryDOBREV, Dobromir; RAVENS, Ursula; ABBATE, Rosanna et al.European heart journal. 2006, Vol 27, Num 14, issn 0195-668X, 1640-1641,1712-1718 [9 p.]Article

MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated PolyposisPIN, Elisa; PASTRELLO, Chiara; MAESTRO, Roberta et al.International journal of cancer (Print). 2013, Vol 132, Num 5, pp 1060-1069, issn 0020-7136, 10 p.Article

Endothelial nitric oxide synthase gene influences the risk of pre-eclampsia, the recurrence of negative pregnancy events, and the maternal-fetal flowFATINI, Cinzia; STICCHI, Elena; GENSINI, Francesca et al.Journal of hypertension. 2006, Vol 24, Num 9, pp 1823-1829, issn 0263-6352, 7 p.Article

BRCA1-related malignancies in a family presenting with von Recklinghausen's diseaseCECCARONI, Marcello; GENUARDI, Maurizio; LEGGE, Francesco et al.Gynecologic oncology (Print). 2002, Vol 86, Num 3, pp 375-378, issn 0090-8258Article

The policy of public health genomics in ItalySIMONE, Benedetto; MAZZUCCO, Walter; VARESCO, Liliana et al.Health policy (Amsterdam. Print). 2013, Vol 110, Num 2-3, pp 214-219, issn 0168-8510, 6 p.Article

Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central ItalyPAPI, Laura; PUTIGNANO, Anna Laura; GENUARDI, Maurizio et al.Breast cancer research and treatment. 2009, Vol 117, Num 3, pp 497-504, issn 0167-6806, 8 p.Article

Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancerPONZ DE LEON, Maurizio; BENATTI, Piero; RONCUCCI, Luca et al.Scandinavian journal of gastroenterology. 2007, Vol 42, Num 6, pp 746-753, issn 0036-5521, 8 p.Article

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