Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease

Author:

Rasmussen Astrid,Alonso Elisa,Ochoa Adriana,De Biase Irene,Familiar Itziar,Yescas Petra,Sosa Ana-Luisa,Rodríguez Yaneth,Chávez Mireya,López-López Marisol,Bidichandani Sanjay I

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference31 articles.

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2. Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavaè D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M: Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat. 1996, 8: 348-357. 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3.

3. Lips CJM: Clinical Management of the multiple endocrine neoplasia syndromes: results of a computerized opinion poll at the Sixth International Workshop on Multiple Endocrine Neoplasia and von Hippel-Lindau disease. J Intern Med. 1998, 243: 589-594. 10.1046/j.1365-2796.1998.00375.x.

4. Burke W, Press N: Genetics as a tool to improve cancer outcomes: ethics and policy. Nature Rev Cancer. 2006, 6: 476-482. 10.1038/nrc1890.

5. Fannos JH: Developmental tasks of childhood and adolescence: Implications for genetic testing. Am J Med Genet. 1997, 71: 22-28. 10.1002/(SICI)1096-8628(19970711)71:1<22::AID-AJMG4>3.0.CO;2-S.

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