158 related articles for article (PubMed ID: 9321761)
21. von Hippel-Lindau disease and familial polyposis coli in the same family.
Kilmartin DJ; Mooney DJ; Acheson RW; Payne SJ; Maher ER; Eustace P
Arch Ophthalmol; 1996 Oct; 114(10):1294. PubMed ID: 8859104
[No Abstract] [Full Text] [Related]
22. Update on the management of familial central nervous system tumor syndromes.
Hottinger AF; Khakoo Y
Curr Neurol Neurosci Rep; 2007 May; 7(3):200-7. PubMed ID: 17488585
[TBL] [Abstract][Full Text] [Related]
23. [Molecular genetics of familial tumour syndromes of the central nervous system].
Murnyák B; Szepesi R; Hortobágyi T
Orv Hetil; 2015 Feb; 156(5):171-7. PubMed ID: 25618858
[TBL] [Abstract][Full Text] [Related]
24. Neurooncology of familial cancer syndromes.
Hottinger AF; Khakoo Y
J Child Neurol; 2009 Dec; 24(12):1526-35. PubMed ID: 19955345
[TBL] [Abstract][Full Text] [Related]
25. High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer.
Mork ME; You YN; Ying J; Bannon SA; Lynch PM; Rodriguez-Bigas MA; Vilar E
J Clin Oncol; 2015 Nov; 33(31):3544-9. PubMed ID: 26195711
[TBL] [Abstract][Full Text] [Related]
26. p.N78S and p.R161Q germline mutations of the VHL gene are present in von Hippel-Lindau syndrome in two pedigrees.
Qi XP; Liu WT; Li JY; Dai Y; Ma JM; Zhao Y; Fei J; Li F; Shen M; Jin HY; Chen ZG; Du ZF; Chen XL; Zhang XN
Mol Med Rep; 2013 Sep; 8(3):799-805. PubMed ID: 23842656
[TBL] [Abstract][Full Text] [Related]
27. Genetic testing by cancer site: colon (polyposis syndromes).
Jasperson KW
Cancer J; 2012; 18(4):328-33. PubMed ID: 22846733
[TBL] [Abstract][Full Text] [Related]
28. Whole-exome analysis of a Li-Fraumeni family trio with a novel TP53 PRD mutation and anticipation profile.
Franceschi S; Spugnesi L; Aretini P; Lessi F; Scarpitta R; Galli A; Congregati C; Caligo MA; Mazzanti CM
Carcinogenesis; 2017 Sep; 38(9):938-943. PubMed ID: 28911001
[TBL] [Abstract][Full Text] [Related]
29. [Familial colorectal cancer].
Sunde LE; Bülow S; Bernstein IT
Ugeskr Laeger; 2006 Jun; 168(24):2369-73. PubMed ID: 16822423
[TBL] [Abstract][Full Text] [Related]
30. Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
Dommering CJ; Henneman L; van der Hout AH; Jonker MA; Tops CM; van den Ouweland AM; van der Luijt RB; Mensenkamp AR; Hogervorst FB; Redeker EJ; de Die-Smulders CE; Moll AC; Meijers-Heijboer H
Fam Cancer; 2017 Apr; 16(2):271-277. PubMed ID: 27826806
[TBL] [Abstract][Full Text] [Related]
31. [Specialized genetic counseling in pediatric and adult oncology patients].
Krutílková V; Havlovicová M; Goetz P
Cas Lek Cesk; 2002; 141(1):23-7. PubMed ID: 11899542
[TBL] [Abstract][Full Text] [Related]
32. Tumor Syndromes: Neurosurgical Evaluation and Management.
Ganapathy A; Diaz EJ; Coleman JT; Mackey KA
Neurosurg Clin N Am; 2022 Jan; 33(1):91-104. PubMed ID: 34801146
[TBL] [Abstract][Full Text] [Related]
33. Familial adenomatous polyposis in pediatrics: natural history, emerging surveillance and management protocols, chemopreventive strategies, and areas of ongoing debate.
Septer S; Lawson CE; Anant S; Attard T
Fam Cancer; 2016 Jul; 15(3):477-85. PubMed ID: 27056662
[TBL] [Abstract][Full Text] [Related]
34. Neurofibromatosis type 2 and von Hippel-Lindau disease: from gene cloning to function.
Kley N; Whaley J; Seizinger BR
Glia; 1995 Nov; 15(3):297-307. PubMed ID: 8586465
[TBL] [Abstract][Full Text] [Related]
35. Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil.
Giacomazzi J; Selistre SG; Rossi C; Alemar B; Santos-Silva P; Pereira FS; Netto CB; Cossio SL; Roth DE; Brunetto AL; Zagonel-Oliveira M; Martel-Planche G; Goldim JR; Hainaut P; Camey SA; Ashton-Prolla P
Cancer; 2013 Dec; 119(24):4341-9. PubMed ID: 24122735
[TBL] [Abstract][Full Text] [Related]
36. Familial cancer syndromes and clusters.
Birch JM
Br Med Bull; 1994 Jul; 50(3):624-39. PubMed ID: 7987644
[TBL] [Abstract][Full Text] [Related]
37. Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
Maher ER; Webster AR; Richards FM; Green JS; Crossey PA; Payne SJ; Moore AT
J Med Genet; 1996 Apr; 33(4):328-32. PubMed ID: 8730290
[TBL] [Abstract][Full Text] [Related]
38. Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
Lammens CR; Aaronson NK; Wagner A; Sijmons RH; Ausems MG; Vriends AH; Ruijs MW; van Os TA; Spruijt L; Gómez García EB; Kluijt I; Nagtegaal T; Verhoef S; Bleiker EM
J Clin Oncol; 2010 Jun; 28(18):3008-14. PubMed ID: 20479422
[TBL] [Abstract][Full Text] [Related]
39. The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis.
Duncan RE; Gillam L; Savulescu J; Williamson R; Rogers JG; Delatycki MB
Fam Cancer; 2010 Mar; 9(1):27-35. PubMed ID: 19760114
[TBL] [Abstract][Full Text] [Related]
40. Challenges in the genetic testing of children for familial cancers.
Clarke AJ; Gaff C
Arch Dis Child; 2008 Nov; 93(11):911-4. PubMed ID: 18941019
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]