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Authors: Jarvinen, O Lehesjoki, AE Lindlof, M Uutela, A Kaariainen, H
Citation: O. Jarvinen et al., Carrier testing of children for two X-linked diseases: A retrospective study of comprehension of the test results and social and psychological significance of the testing, PEDIATRICS, 106(6), 2000, pp. 1460-1465

Authors: Jarvinen, O Aalto, AM Lehesjoki, AE Lindlof, M Soderling, I Uutela, A Kaariainen, H
Citation: O. Jarvinen et al., Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation, J MED GENET, 36(8), 1999, pp. 615-620

Authors: Karenko, L Kahkonen, M Hyytinen, ER Lindlof, M Ranki, A
Citation: L. Karenko et al., Notable losses at specific regions of chromosomes 10q and 13q in the Sezary syndrome detected by comparative genomic hybridization, J INVES DER, 112(3), 1999, pp. 392-395

Authors: Watowich, SS Xie, XL Klingmuller, U Kere, J Lindlof, M Berglund, S de la Chapelle, A
Citation: Ss. Watowich et al., Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state, BLOOD, 94(7), 1999, pp. 2530-2532
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