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2. Human genetics. Neurofibromatosis gene cloned. Ponder B Nature; 1990 Aug; 346(6286):703-4. PubMed ID: 2117711 [No Abstract] [Full Text] [Related]
3. Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication. Kehrer-Sawatzki H; Assum G; Hameister H Hum Genet; 2002 Oct; 111(4-5):465-7; author reply 468-9. PubMed ID: 12384794 [TBL] [Abstract][Full Text] [Related]
4. Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14. Verhest A; Heimann R; Verschraegen J; Vamos E; Hecht F Neurofibromatosis; 1988; 1(1):33-6. PubMed ID: 3152526 [TBL] [Abstract][Full Text] [Related]
5. Progress towards the isolation and characterization of the genes causing neurofibromatosis. Menon AG; Gusella JF; Seizinger BR Cancer Surv; 1990; 9(4):689-702. PubMed ID: 2129297 [TBL] [Abstract][Full Text] [Related]
6. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Legius E; Marchuk DA; Collins FS; Glover TW Nat Genet; 1993 Feb; 3(2):122-6. PubMed ID: 8499945 [TBL] [Abstract][Full Text] [Related]
7. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Viskochil D; Buchberg AM; Xu G; Cawthon RM; Stevens J; Wolff RK; Culver M; Carey JC; Copeland NG; Jenkins NA Cell; 1990 Jul; 62(1):187-92. PubMed ID: 1694727 [TBL] [Abstract][Full Text] [Related]
8. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients. Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774 [TBL] [Abstract][Full Text] [Related]
9. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma]. Laureys GG Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670 [TBL] [Abstract][Full Text] [Related]
11. The neurofibromatosis type 1 gene. Viskochil D; White R; Cawthon R Annu Rev Neurosci; 1993; 16():183-205. PubMed ID: 8460890 [No Abstract] [Full Text] [Related]
12. Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma. Lekanne Deprez RH; Riegman PH; Groen NA; Warringa UL; van Biezen NA; Molijn AC; Bootsma D; de Jong PJ; Menon AG; Kley NA Oncogene; 1995 Apr; 10(8):1521-8. PubMed ID: 7731706 [TBL] [Abstract][Full Text] [Related]
13. [From gene to disease; neurofibromatosis type 1]. de Goede-Bolder A; Cnossen MH; Dooijes D; van den Ouweland AM; Niermeijer MF Ned Tijdschr Geneeskd; 2001 Sep; 145(36):1736-8. PubMed ID: 11572174 [TBL] [Abstract][Full Text] [Related]
14. Neurofibromatosis 2 (bilateral acoustic schwannomas). What is it? A review of literature and an update. Desouza CE; Nagpal RD J Postgrad Med; 1992; 38(1):27-31. PubMed ID: 1512722 [No Abstract] [Full Text] [Related]
15. Involvement of 22q12 in a neurofibrosarcoma in neurofibromatosis type 1. Rey JA; Bello MJ; Kusak ME; de Campos JM; PestaƱa A Cancer Genet Cytogenet; 1993 Mar; 66(1):28-32. PubMed ID: 8467471 [TBL] [Abstract][Full Text] [Related]
16. Neurofibromatosis genetic study. Gardner RJ; Hughes PM; Lovell-Smith CJ; Chapman CJ N Z Med J; 1988 Dec; 101(859):832. PubMed ID: 3144682 [No Abstract] [Full Text] [Related]
17. 17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one. Asamoah A; North K; Doran S; Wagstaff J; Ogle R; Collins FS; Korf BR Am J Med Genet; 1995 Aug; 60(4):312-6. PubMed ID: 7485267 [TBL] [Abstract][Full Text] [Related]
18. Neurofibromatosis type 1. Legius E; Descheemaeker MJ; Fryns JP; Van den Berghe H Genet Couns; 1994; 5(3):225-41. PubMed ID: 7811422 [TBL] [Abstract][Full Text] [Related]
19. DNA deletion in patients with von Recklinghausen neurofibromatosis. Kamei T; Fukushima Y; Shibata A; Hayashi Y; Tachibana N; Takeda I; Niikawa N; Collins FS; Takahashi K; Masumura S Clin Genet; 1992 Jul; 42(1):53-4. PubMed ID: 1516229 [No Abstract] [Full Text] [Related]
20. Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association. Bahuau M; Flintoff W; Assouline B; Lyonnet S; Le Merrer M; Prieur M; Guilloud-Bataille M; Feingold N; Munnich A; Vidaud M; Vidaud D Am J Med Genet; 1996 Dec; 66(3):347-55. PubMed ID: 8985499 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]