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238 related items for PubMed ID: 32239880
1. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Kuiper RP, Nielsen M, De Voer RM, Hoogerbrugge N. ; 1993. PubMed ID: 32239880 [Abstract] [Full Text] [Related]
2. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Nielsen M, Infante E, Brand R. ; 1993. PubMed ID: 23035301 [Abstract] [Full Text] [Related]
7. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Larsen Haidle J, MacFarland SP, Howe JR. ; 1993. PubMed ID: 20301642 [Abstract] [Full Text] [Related]
8. Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium. Boulouard F, Kasper E, Buisine MP, Lienard G, Vasseur S, Manase S, Bahuau M, Barouk Simonet E, Bubien V, Coulet F, Cusin V, Dhooge M, Golmard L, Goussot V, Hamzaoui N, Lacaze E, Lejeune S, Mauillon J, Beaumont MP, Pinson S, Tlemsani C, Toulas C, Rey JM, Uhrhammer N, Bougeard G, Frebourg T, Houdayer C, Baert-Desurmont S. Clin Genet; 2021 May; 99(5):662-672. PubMed ID: 33454955 [Abstract] [Full Text] [Related]
9. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Schneider K, Zelley K, Nichols KE, Schwartz Levine A, Garber J. ; 1993 May. PubMed ID: 20301488 [Abstract] [Full Text] [Related]
10. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lohmann DR, Gallie BL. ; 1993 May. PubMed ID: 20301625 [Abstract] [Full Text] [Related]
11. Familial adenomatous polyposis. Half E, Bercovich D, Rozen P. Orphanet J Rare Dis; 2009 Oct 12; 4():22. PubMed ID: 19822006 [Abstract] [Full Text] [Related]
12. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Nelson A, Myers K. ; 1993 Oct 12. PubMed ID: 20301722 [Abstract] [Full Text] [Related]
13. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Langer K, Cunniff CM, Kucine N. ; 1993 Oct 12. PubMed ID: 20301572 [Abstract] [Full Text] [Related]
14. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Yehia L, Eng C. ; 1993 Oct 12. PubMed ID: 20301661 [Abstract] [Full Text] [Related]
15. NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas. Belhadj S, Quintana I, Mur P, Munoz-Torres PM, Alonso MH, Navarro M, Terradas M, Piñol V, Brunet J, Moreno V, Lázaro C, Capellá G, Valle L. Sci Rep; 2019 Jun 21; 9(1):9020. PubMed ID: 31227763 [Abstract] [Full Text] [Related]
16. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Schultz KAP, Stewart DR, Kamihara J, Bauer AJ, Merideth MA, Stratton P, Huryn LA, Harris AK, Doros L, Field A, Carr AG, Dehner LP, Messinger Y, Hill DA. ; 1993 Jun 21. PubMed ID: 24761742 [Abstract] [Full Text] [Related]
17. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Langer AL. ; 1993 Jun 21. PubMed ID: 20301599 [Abstract] [Full Text] [Related]
18. Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review. Beck SH, Jelsig AM, Yassin HM, Lindberg LJ, Wadt KAW, Karstensen JG. Fam Cancer; 2022 Oct 21; 21(4):453-462. PubMed ID: 35292903 [Abstract] [Full Text] [Related]
19. Six case reports of NTHL1-associated tumor syndrome further support it as a multi-tumor predisposition syndrome. Weatherill CB, Burke SA, Haskins CG, Berry DK, Homer JP, Demeure MJ, Darabi S. Clin Genet; 2023 Feb 21; 103(2):231-235. PubMed ID: 36196035 [Abstract] [Full Text] [Related]
20. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Marzin P, Cormier-Daire V. ; 1993 Feb 21. PubMed ID: 20301776 [Abstract] [Full Text] [Related] Page: [Next] [New Search]