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Autor:
Afaya, Agani, Kim, Sung-Won, Park, Hyung Seok, Lim, Myong Cheol, Jung, Mi Sook, Nam, Eun Ji, Park, Ji Soo, Jeong, Joon, Ryu, Jai Min, Kim, JiSun, Kim, Jihye, Kim, Minkyoung, Jin, Juhye, Han, Jeehee, Kim, Soo Yeon, Park, Sun-Young, Katapodi, Maria C., Kim, Sue
Publikováno v:
Familial Cancer; Jun2024, Vol. 23 Issue 2, p121-132, 12p
Autor:
Toh, Ming Ren, Low, Chen Ee, Chong, Siao Ting, Chan, Sock Hoai, Ishak, Nur Diana Binte, Courtney, Eliza, Kolinjivadi, Arun Mouli, Rodrigue, Amélie, Masson, Jean-Yves, Ngeow, Joanne
Publikováno v:
Familial Cancer; Apr2020, Vol. 19 Issue 2, p123-131, 9p
Autor:
Serena Masciari, Niki Boyd, Sara Wiyrick, Pardeep Kaurah, Janine Senz, Wylie Burke, Henry Lynch, Judy Garber
Publikováno v:
Familial Cancer; Mar2008, Vol. 7 Issue 1, p73-82, 10p, 2 Diagrams, 1 Chart
Publikováno v:
Familial Cancer; Dec2007, Vol. 6 Issue 4, p415-443, 29p
Autor:
Mariëlle Ruijs, Senno Verhoef, Gea Wigbout, Roelof Pruntel, Arno Floore, Daphne de Jong, Laura van ′t Veer, Fred Menko
Publikováno v:
Familial Cancer; Jun2006, Vol. 5 Issue 2, p169-174, 6p
Autor:
Jan Steffen, Michalina Dabrowska, Aneta Balabas, Magdalena Piatkowska, Dorota Nowakowska, Izabela Brozek, Anna Niwińska, Magdalena Ratajska, Jadwiga Rachtan, Janusz Limon, Anna Kluska
Publikováno v:
Familial Cancer
It is estimated that about 5–10% of ovarian and 2–5% of all breast cancer patients are carriers of a germline BRCA1 or BRCA2 gene mutation. Most families with detected BRCA1 or BRCA2 gene mutation are qualified for molecular testing on the basis