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