These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
173 related articles for article (PubMed ID: 2014801)
21. Large-scale physical mapping within the region 22q12.3-13.1 in meningioma. Herzog R; Gottert E; Henn W; Zang K; Blin N; Trent J; Meese E Genomics; 1991 Aug; 10(4):1041-6. PubMed ID: 1916810 [TBL] [Abstract][Full Text] [Related]
22. Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor. Newsham I; Daub D; Besnard-Guerin C; Cavenee W Genomics; 1994 Feb; 19(3):433-40. PubMed ID: 8188285 [TBL] [Abstract][Full Text] [Related]
23. Age associated increase in the prevalence of chromosome 22q loss of heterozygosity in histological subsets of benign meningioma. Baser ME; Poussaint TY J Med Genet; 2006 Mar; 43(3):285-7. PubMed ID: 15980114 [TBL] [Abstract][Full Text] [Related]
24. Molecular genetic analysis of chromosome 22 in 81 cases of meningioma. Dumanski JP; Rouleau GA; Nordenskjöld M; Collins VP Cancer Res; 1990 Sep; 50(18):5863-7. PubMed ID: 2393856 [TBL] [Abstract][Full Text] [Related]
25. Variant Ph1 translocations in CML and their incidence, including two cases with sequential lymphoid and myeloid crises. Oshimura M; Ohyashiki K; Terada H; Takaku F; Tonomura A Cancer Genet Cytogenet; 1982 Mar; 5(3):187-201. PubMed ID: 6950809 [TBL] [Abstract][Full Text] [Related]
26. Familial meningioma is not allelic to neurofibromatosis 2. Pulst SM; Rouleau GA; Marineau C; Fain P; Sieb JP Neurology; 1993 Oct; 43(10):2096-8. PubMed ID: 8413972 [TBL] [Abstract][Full Text] [Related]
27. The genes for the highly homologous Ca(2+)-binding proteins oncomodulin and parvalbumin are not linked in the human genome. Ritzler JM; Sawhney R; Geurts van Kessel AH; Grzeschik KH; Schinzel A; Berchtold MW Genomics; 1992 Mar; 12(3):567-72. PubMed ID: 1559707 [TBL] [Abstract][Full Text] [Related]
28. Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid. Cox DR; Pritchard CA; Uglum E; Casher D; Kobori J; Myers RM Genomics; 1989 Apr; 4(3):397-407. PubMed ID: 2523853 [TBL] [Abstract][Full Text] [Related]
29. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report. Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036 [TBL] [Abstract][Full Text] [Related]
30. Duplication of distal 22q. Abeliovich D; Maor E; Bashan N; Carmi R Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354 [TBL] [Abstract][Full Text] [Related]
31. A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene. Wasmuth JJ; Carlock LR; Smith B; Immken LL Am J Hum Genet; 1986 Sep; 39(3):397-403. PubMed ID: 2945430 [TBL] [Abstract][Full Text] [Related]
32. The t(11;22)(p15.5;q11.23) in a retroperitoneal rhabdoid tumor also includes a regional deletion distal to CRYBB2 on 22q. Besnard-Guérin C; Cavenee W; Newsham I Genes Chromosomes Cancer; 1995 Jul; 13(3):145-50. PubMed ID: 7669732 [TBL] [Abstract][Full Text] [Related]
33. A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus. Frazer KA; Boehnke M; Budarf ML; Wolff RK; Emanuel BS; Myers RM; Cox DR Genomics; 1992 Nov; 14(3):574-84. PubMed ID: 1427886 [TBL] [Abstract][Full Text] [Related]
34. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte. Simi P; Ceccarelli M; Barachini A; Floridia G; Zuffardi O Hum Genet; 1992 Feb; 88(4):482-3. PubMed ID: 1740326 [TBL] [Abstract][Full Text] [Related]
35. A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene. MacDonald ME; Anderson MA; Gilliam TC; Tranejaerg L; Carpenter NJ; Magenis E; Hayden MR; Healey ST; Bonner TI; Gusella JF Genomics; 1987 Sep; 1(1):29-34. PubMed ID: 2889660 [TBL] [Abstract][Full Text] [Related]
36. Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics. Mocker K; Holland H; Ahnert P; Schober R; Bauer M; Kirsten H; Koschny R; Meixensberger J; Krupp W Pathol Res Pract; 2011 Jan; 207(1):67-72. PubMed ID: 20926204 [TBL] [Abstract][Full Text] [Related]
37. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q. Lindblom A; Sandelin K; Iselius L; Dumanski J; White I; Nordenskjöld M; Larsson C Am J Hum Genet; 1994 May; 54(5):871-6. PubMed ID: 8178827 [TBL] [Abstract][Full Text] [Related]
38. The generation of DNA probes to chromosome 11q23 by Alu PCR on small numbers of flow-sorted 22q- derivative chromosomes. Cotter FE; Das S; Douek E; Carter NP; Young BD Genomics; 1991 Mar; 9(3):473-80. PubMed ID: 2032719 [TBL] [Abstract][Full Text] [Related]
39. Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas. Papi L; De Vitis LR; Vitelli F; Ammannati F; Mennonna P; Montali E; Bigozzi U Hum Genet; 1995 Mar; 95(3):347-51. PubMed ID: 7868131 [TBL] [Abstract][Full Text] [Related]
40. Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line. Reynolds JE; Fletcher JA; Lytle CH; Nie L; Morton CC; Diehl SR Hum Genet; 1992 Dec; 90(4):450-6. PubMed ID: 1483704 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]