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The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions.
Kehrer-Sawatzki, H; Häussler, J; Krone, W; Bode, H; Jenne, D E; Mehnert, K U; Tümmers, U; Assum, G.
Affiliation
  • Kehrer-Sawatzki H; Abteilung Humangenetik, Ulm, Germany.
Hum Genet ; 99(2): 237-47, 1997 Feb.
Article in En | MEDLINE | ID: mdl-9048928
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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 17 / Chromosomes, Human, Pair 22 / Neurofibromatosis 1 Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans Language: En Journal: Hum Genet Year: 1997 Document type: Article
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 17 / Chromosomes, Human, Pair 22 / Neurofibromatosis 1 Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans Language: En Journal: Hum Genet Year: 1997 Document type: Article