The American founder mutation for Lynch syndrome: Prevalence and cancer control implications.

被引:0
|
作者
Lynch, HT
de la Chapelle, A
Hampel, H
Wagner, A
Fodde, R
Okimoto, R
Clark, MB
Coronel, S
Trowonou, A
Haynatzki, GR
Gong, G
机构
[1] Creighton Univ, Omaha, NE 68178 USA
[2] Ohio State Univ, Columbus, OH 43210 USA
[3] Erasmus Univ, Med Ctr, Rotterdam, Netherlands
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:838S / 838S
页数:1
相关论文
共 50 条
  • [1] American founder mutation for Lynch syndrome - Prevalence estimates and implications
    Lynch, HT
    de la Chapelle, A
    Hampel, H
    Wagner, A
    Fodde, R
    Lynch, JF
    Okimoto, R
    Clark, MB
    Coronel, S
    Trowonou, A
    Fu, YX
    Haynatzki, GR
    Gong, G
    [J]. CANCER, 2006, 106 (02) : 448 - 452
  • [2] Founder mutation in Lynch syndrome
    Cajal, Andrea R.
    Pinero, Tamara A.
    Verzura, Alicia
    Pablo Santino, Juan
    Solano, Angela R.
    Kalfayan, Pablo G.
    Ferro, Alejandra
    Vaccaro, Carlos
    [J]. MEDICINA-BUENOS AIRES, 2016, 76 (03) : 180 - 182
  • [3] Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation
    Christina Therkildsen
    Anna Isinger-Ekstrand
    Steen Ladelund
    Anja Nissen
    Eva Rambech
    Inge Bernstein
    Mef Nilbert
    [J]. Familial Cancer, 2012, 11 : 579 - 585
  • [4] Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation
    Therkildsen, Christina
    Isinger-Ekstrand, Anna
    Ladelund, Steen
    Nissen, Anja
    Rambech, Eva
    Bernstein, Inge
    Nilbert, Mef
    [J]. FAMILIAL CANCER, 2012, 11 (04) : 579 - 585
  • [5] Mutation Spectrum and Risk of Colorectal Cancer in African American Families with Lynch Syndrome
    Guindalini, Rodrigo Santa Cruz
    Win, Aung Ko
    Gulden, Cassandra
    Lindor, Noralane M.
    Newcomb, Polly A.
    Haile, Robert W.
    Raymond, Victoria
    Stoffel, Elena
    Hall, Michael
    Llor, Xavier
    Ukaegbu, Chinedu I.
    Solomon, Ilana
    Weitzel, Jeffrey
    Kalady, Matthew
    Blanco, Amie
    Terdiman, Jonathan
    Shuttlesworth, Gladis A.
    Lynch, Patrick M.
    Hampel, Heather
    Lynch, Henry T.
    Jenkins, Mark A.
    Olopade, Olufunmilayo I.
    Kupfer, Sonia S.
    [J]. GASTROENTEROLOGY, 2015, 149 (06) : 1446 - 1453
  • [6] Mutation prevalence in a large series of patients with Lynch Syndrome
    Martin, M.
    Burbidge, L.
    Frye, C.
    Roa, B.
    Wenstrup, R.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (15)
  • [7] A novel founder mutation in variegate porphyria patients from Chile and its future implications.
    Frank, J
    Aita, VM
    Ahmad, W
    Lam, H
    Wolff, C
    Christiano, AM
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A203 - A203
  • [8] Mutation spectrum in South American Lynch syndrome families
    Mev Dominguez-Valentin
    Mef Nilbert
    Patrik Wernhoff
    Francisco López-Köstner
    Carlos Vaccaro
    Carlos Sarroca
    Edenir Ines Palmero
    Alejandro Giraldo
    Patricia Ashton-Prolla
    Karin Alvarez
    Alejandra Ferro
    Florencia Neffa
    Junea Caris
    Dirce M Carraro
    Benedito M Rossi
    [J]. Hereditary Cancer in Clinical Practice, 11
  • [9] Mutation spectrum in South American Lynch syndrome families
    Dominguez-Valentin, Mev
    Nilbert, Mef
    Wernhoff, Patrik
    Lopez-Koestner, Francisco
    Vaccaro, Carlos
    Sarroca, Carlos
    Palmero, Edenir Ines
    Giraldo, Alejandro
    Ashton-Prolla, Patricia
    Alvarez, Karin
    Ferro, Alejandra
    Neffa, Florencia
    Caris, Junea
    Carraro, Dirce M.
    Rossi, Benedito M.
    [J]. HEREDITARY CANCER IN CLINICAL PRACTICE, 2013, 11
  • [10] Origins and prevalence of the American Founder Mutation of MSH2
    Clendenning, Mark
    Baze, Mark E.
    Sun, Shuying
    Walsh, Kyle
    Liyanarachchi, Sandya
    Fix, Dan
    Schunemann, Victoria
    Comeras, Ilene
    Deacon, Molly
    Lynch, Jane F.
    Gong, Gordon
    Thomas, Brittany C.
    Thibodeau, Stephen N.
    Lynch, Henry T.
    Hampel, Heather
    De la Chapelle, Albert
    [J]. CANCER RESEARCH, 2008, 68 (07) : 2145 - 2153