Increased prevalence of overweight in adolescent girls with type 1 diabetes mellitus von DOMARGARD, A, SÄRNBLAD, S, KROON, M, KARLSSON, I, SKEPPNER, G, AMAN, J

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Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb von Willig, Thiébaut-Noel, Haeringen, Arie van, Veer-Korthof, Lisbeth van't, Tchernia, Gil, Gordon, Laurie, Dianzani, Irma, Renter, Jan-Inge, Donnér, Mikael, Nilsson, Per-Gunnar, Gustavsson, Peter, Dahl, Niklas, Elinder, Göran, Skeppner, Gunnar, Kreuger, Anders

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Febrile Plasmodium falciparum Malaria 4 Years after Exposure in a Man with Sickle Cell Disease von Greenwood, Tatiana, Vikerfors, Tomas, Sjöberg, Maria, Skeppner, Gunnar, Färnert, Anna

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Sequential Combined Spinal Epidural Block Versus Spinal Block for Cesarean Section: Effects on Maternal Hypotension and Neurobehavioral Function of the Newborn von Thorén, Titti, Holmström, Björn, Rawal, Narinder, Schollin, Jens, Lindeberg, Solveig, Skeppner, Gunnar

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Transient red cell aplasia in siblings: a common environmental or a common hereditary factor? von Skeppner, G, Forestier, E, Henter, JI, Wranne, L

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Transient erythroblastopenia of childhood: Prospective study of 10 patients with special reference to viral infections von SKEPPNER, Gunnar, KREUGER, Anders, ELINDER, Goran

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Diamond-Blackfan anaemia in a girl with a de novo balanced reciprocal X;19 translocation von Gustavsson, P, Skeppner, G, Johansson, B, Berg, T, Gordon, L, Kreuger, A, Dahl, N

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Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RP... von Gustavsson, Peter, Klar, Joakim, Matsson, Hans, Forestier, Erik, Henter, Jan‐Inge, Rao, Sreedhar, Seip, Martin, Skeppner, Gunnar, Dahl, Niklas

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TRANSIENT RED CELL APLASIA IN SIBLINGS: A RESULT OF COMMON INHERITAGE? 143 von Skeppner, G, Forestier, E, Henter, J-I, Wranne, L

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Increased prevalence of overweight in adolescent girls with type 1 diabetes mellitus von Domargård, A, Särnblad, S, Kroon, M, Karlsson, I, Skeppner, G, Åman, J

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Transient red cell aplasia in siblings: a common environmental or a common hereditary factor? von Skeppner, G, Forestier, E, Henter, J-I, Wranne, L

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Genetics of Diamond-Blackfan anemia: Analysis of the chromosome 19q13.2 region in familial and sporadic cases von Gustavsson, P, Garelli, E, Draptchinskaia, N, Ball, S, Willig, TN, Ramenghi, U, Dianzani, I, Goringe, A, Olivieri, NF, Smibert, E, Tchernia, G, Elinder, G, Skeppner, G, Dahl, N

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