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Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity.
Gustavsson, P; Garelli, E; Draptchinskaia, N; Ball, S; Willig, T N; Tentler, D; Dianzani, I; Punnett, H H; Shafer, F E; Cario, H; Ramenghi, U; Glomstein, A; Pfeiffer, R A; Goringe, A; Olivieri, N F; Smibert, E; Tchernia, G; Elinder, G; Dahl, N.
Affiliation
  • Gustavsson P; Unit of Clinical Genetics, Department of Genetics and Pathology, Uppsala University Children's Hospital, Uppsala, Sweden.
Am J Hum Genet ; 63(5): 1388-95, 1998 Nov.
Article in En | MEDLINE | ID: mdl-9792865
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Chromosomes, Human, Pair 19 / Sequence Deletion / Fanconi Anemia Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1998 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Chromosomes, Human, Pair 19 / Sequence Deletion / Fanconi Anemia Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1998 Document type: Article