365 related articles for article (PubMed ID: 28411145)
41. Cost-Effectiveness Analysis of Different Genetic Testing Strategies for Lynch Syndrome in Taiwan.
Chen YE; Kao SS; Chung RH
PLoS One; 2016; 11(8):e0160599. PubMed ID: 27482709
[TBL] [Abstract][Full Text] [Related]
42. Prophylactic Gynecologic Specimens from Hereditary Cancer Carriers.
Shaw PA; Clarke BA
Surg Pathol Clin; 2016 Jun; 9(2):307-28. PubMed ID: 27241111
[TBL] [Abstract][Full Text] [Related]
43. Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.
Skeldon SC; Semotiuk K; Aronson M; Holter S; Gallinger S; Pollett A; Kuk C; van Rhijn B; Bostrom P; Cohen Z; Fleshner NE; Jewett MA; Hanna S; Shariat SF; Van Der Kwast TH; Evans A; Catto J; Bapat B; Zlotta AR
Eur Urol; 2013 Feb; 63(2):379-85. PubMed ID: 22883484
[TBL] [Abstract][Full Text] [Related]
44. ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal S; Brand RE; Church JM; Giardiello FM; Hampel HL; Burt RW;
Am J Gastroenterol; 2015 Feb; 110(2):223-62; quiz 263. PubMed ID: 25645574
[TBL] [Abstract][Full Text] [Related]
45. [Hereditary predispositions to gynaecological cancers].
Coupier I; Pujol P
Gynecol Obstet Fertil; 2005 Nov; 33(11):851-6. PubMed ID: 16256400
[TBL] [Abstract][Full Text] [Related]
46. Genetic mutation risk calculation in Lynch syndrome inheritance: Evaluating the utility of the PREMM
Aissaoui S; Cartellier C; Seytier T; Giraud S; Calender A
Bull Cancer; 2017 Mar; 104(3):288-294. PubMed ID: 28038733
[TBL] [Abstract][Full Text] [Related]
47. Gastric cancer in Lynch syndrome is associated with underlying immune gastritis.
Adar T; Friedman M; Rodgers LH; Shannon KM; Zukerberg LR; Chung DC
J Med Genet; 2019 Dec; 56(12):844-845. PubMed ID: 31055502
[No Abstract] [Full Text] [Related]
48. Cancer genetics and reproduction.
Hanson H; Hodgson S
Best Pract Res Clin Obstet Gynaecol; 2010 Feb; 24(1):3-18. PubMed ID: 19864186
[TBL] [Abstract][Full Text] [Related]
49. Mismatch repair deficiency in Lynch syndrome-associated colorectal adenomas is more prevalent in older patients.
Tanaka M; Nakajima T; Sugano K; Yoshida T; Taniguchi H; Kanemitsu Y; Nagino M; Sekine S
Histopathology; 2016 Aug; 69(2):322-8. PubMed ID: 26826556
[TBL] [Abstract][Full Text] [Related]
50. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.
Walsh T; Casadei S; Coats KH; Swisher E; Stray SM; Higgins J; Roach KC; Mandell J; Lee MK; Ciernikova S; Foretova L; Soucek P; King MC
JAMA; 2006 Mar; 295(12):1379-88. PubMed ID: 16551709
[TBL] [Abstract][Full Text] [Related]
51. Clinical genetics of hereditary colorectal cancer.
Power DG; Gloglowski E; Lipkin SM
Hematol Oncol Clin North Am; 2010 Oct; 24(5):837-59. PubMed ID: 20816577
[TBL] [Abstract][Full Text] [Related]
52. Mismatch repair deficiency testing in clinical practice.
Buza N; Ziai J; Hui P
Expert Rev Mol Diagn; 2016; 16(5):591-604. PubMed ID: 26895074
[TBL] [Abstract][Full Text] [Related]
53. Beyond BRCA1 and BRCA2.
King-Spohn K; Pilarski R
Curr Probl Cancer; 2014; 38(6):235-48. PubMed ID: 25497410
[TBL] [Abstract][Full Text] [Related]
54. Susceptibility to breast cancer: hereditary syndromes and low penetrance genes.
Nusbaum R; Vogel KJ; Ready K
Breast Dis; 2006-2007; 27():21-50. PubMed ID: 17917139
[TBL] [Abstract][Full Text] [Related]
55. Breast cancer predisposition syndromes.
Hemel D; Domchek SM
Hematol Oncol Clin North Am; 2010 Oct; 24(5):799-814. PubMed ID: 20816575
[TBL] [Abstract][Full Text] [Related]
56. The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
Malander S; Rambech E; Kristoffersson U; Halvarsson B; Ridderheim M; Borg A; Nilbert M
Gynecol Oncol; 2006 May; 101(2):238-43. PubMed ID: 16360201
[TBL] [Abstract][Full Text] [Related]
57. Hereditary gastrointestinal cancer.
Hata K; Yamamoto Y; Kiyomatsu T; Tanaka T; Kazama S; Nozawa H; Kawai K; Tanaka J; Nishikawa T; Otani K; Yasuda K; Kishikawa J; Nagai Y; Anzai H; Shinagawa T; Arakawa K; Yamaguchi H; Ishihara S; Sunami E; Kitayama J; Watanabe T
Surg Today; 2016 Oct; 46(10):1115-22. PubMed ID: 26676416
[TBL] [Abstract][Full Text] [Related]
58. [Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: focus on the Peutz-Jeghers].
Turpin A; Cattan S; Leclerc J; Wacrenier A; Manouvrier-Hanu S; Buisine MP; Lejeune-Dumoulin S
Bull Cancer; 2014 Sep; 101(9):813-22. PubMed ID: 25036236
[TBL] [Abstract][Full Text] [Related]
59. Update on Lynch syndrome genomics.
Peltomäki P
Fam Cancer; 2016 Jul; 15(3):385-93. PubMed ID: 26873718
[TBL] [Abstract][Full Text] [Related]
60. Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
Lavoine N; Colas C; Muleris M; Bodo S; Duval A; Entz-Werle N; Coulet F; Cabaret O; Andreiuolo F; Charpy C; Sebille G; Wang Q; Lejeune S; Buisine MP; Leroux D; Couillault G; Leverger G; Fricker JP; Guimbaud R; Mathieu-Dramard M; Jedraszak G; Cohen-Hagenauer O; Guerrini-Rousseau L; Bourdeaut F; Grill J; Caron O; Baert-Dusermont S; Tinat J; Bougeard G; Frébourg T; Brugières L
J Med Genet; 2015 Nov; 52(11):770-8. PubMed ID: 26318770
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]