The history of the Nobel prize for the discovery of insulin von Rydén, Lars, Lindsten, Jan

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Changes in the incidence of Down syndrome in sweden during 1968-1982 von ISELIUS, L, LINDSTEN, J

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European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures von Bui, T.-H., Iselius, L., Lindsten, J.

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The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype: Report of 11 patients an... von Schinzel, A., Schmid, W., Fraccaro, M., Tiepolo, L., Zuffardi, Orsetta, Opitz, J.M., Lindsten, J., Zetterqvist, P., Enell, H., Baccichetti, C., Tenconi, R., Pagon, RobertaA

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The origin and phenotype of XO males von Fraccaro, M, Lindsten, J, Lo Curto, F

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CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILD von Fraccaro, M., Kaijser, K., Lindsten, J.

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CHROMOSOME ABERRATIONS AND SISTER-CHROMATID EXCHANGE IN WORKERS IN CHEMICAL LABORATORIES AND A ROTOPRINTING FACTORY AND IN CHILDREN OF WOMEN LABORATORY WORKERS von Funes-Cravioto, F., Kolmodin-Hedman, B., Lindsten, J., Nordenskjöld, M., Zapata-Gayon, C., Lambert, B., Norberg, E., Olin, R., Swensson, Å.

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NEW TYPE OF CHROMOSOMAL MOSAICISM IN OVARIAN DYSGENESIS von Lindsten, J.

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Maternal smoking during pregnancy and risk of childhood cancer von Stjernfeldt, M, Berglund, K, Lindsten, J, Ludvigsson, J

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Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis von Caspersson, T., Gahrton, G., Lindsten, J., Zech, L.

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The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 families von ISELIUS, L, LINDSTEN, J, DUTRILLAUX, B, FUKUSHIMA, Y, GERAETIS, J. P. M, DE GROUCHY, J, ZUFFARDI, O, AURIAS, A, FRACCARO, M, BASTARD, C, BOTTELLI, A. M, BUI, T.-H, CAUFIN, D, DALPRA, L, DELENDI, N

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A new variant translocation (19q+, 22q−) in chronic myelocytic leukemia von Gahrton, G., Zech, L., Lindsten, J.

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Molecular forms and activities of glycosidases in cultures of amniotic-fluid cells von Hultberg, B, Lindsten, J, Sjöblad, S

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Fluorescent staining of heteropycnotic chromosome regions in human interphase nuclei von Caspersson, T., Zech, L., Johansson, C., Lindsten, J., Hultén, M.

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Methylmercury-induced chromosome damage in man von Skerfving, S., Hansson, K., Mangs, C., Lindsten, J., Ryman, N.

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Evidence for a Major Locus as Well as a Multifactorial Component in the Regulation of Human Red Blood Cell Catechol-O-Methyl-Transferase Activity von Floderus, Y., Iselius, L., Lindsten, J., Wetterberg, L.

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Clonal Origin of the Philadelphia Chromosome From Either the Paternal or the Maternal Chromosome Number 22 von Gahrton, G., Lindsten, J., Zech, L.

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Trisomy 8 in Acute Myeloblastic Leukemia and Sideroachrestic Anemia von Jonasson, J., Gahrton, G., Lindsten, J., Simonsson-Lindemalm, C., Zech, L.

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Correlation between the number of sex chromosomes and the H-Y antigen titer von Fraccaro, M, Mayerová, A, Wolf, U, Bühler, E, Gebauer, J, Gilgenkrantz, S, Lindsten, J, Lo Curto, F, Ritzén, E M

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A Mapping Function for Man von Rao, D. C., Morton, N. E., Lindsten, J., Hultén, M., Yee, S.

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