Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region
Gervasini C, Bentivegna A, Venturin M, Corrado L, Larizza L, Riva P (2002) Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region. Hum Genet 110:314-321
A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions
Jenne DE, Tinschert S, Stegmann E, Reimann H, Nurnberg P, Horn D, Naumann I, Buske A, Thiel G (2000) A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions. Genomics 66:93-97
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions
Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H, Kehrer-Sawatzki H (2001) Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions. Am J Hum Genet 69:516-527
The second case of a t(17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions
Kehrer-Sawatzki H, Haussler J, Krone W, Bode H, Jenne DE, Mehnert KU, Tummers U, Assum G (1997) The second case of a t(17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions. Hum Genet 99:237-247