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J Lindsten

Showing results (61-70 of 131) with videos related to

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Experientia|September 15, 1978
Iron malabsorption and hypochromic anemia in a case of Turner's syndromeT Miale, L Stenke, J Lindsten, et al.
Experimental Cell Research|November 1, 1970
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysisT Caspersson, G Gahrton, J Lindsten, et al.
Cancer Detection and Prevention|January 1, 1992
Maternal smoking and irradiation during pregnancy as risk factors for child leukemiaM Stjernfeldt, K Berglund, J Lindsten, et al.
Human Genetics|January 1, 1982
Data and theory for a revised chiasma map of manN E Morton, J Lindsten, L Iselius, et al.
Human Genetics|January 1, 1980
The 11q;22q translocation: a European collaborative analysis of 43 casesM Fraccaro, J Lindsten, C E Ford, et al.
Hereditas|January 1, 1978
Protein binding of ampicillin. Path analysis of a twin materialL Iselius, M Ehrnebo, L O Boréus, et al.
Behavior Genetics|March 1, 1973
An explanation of the apparently increased incidence of moderate mental retardation in Turner's syndromeD C Garron, L Molander, B Cronholm, et al.
Lakartidningen|May 10, 1972
[Prenatal diagnosis of genetic diseases]B Kjessler, J Lindsten, R Zetterström, et al.
Lakartidningen|January 22, 1975
[Prenatal diagnosis of anencephalus and spina bifida by determination of alphafetoprotein]B Hellström, J Lindsten, L Marsk, et al.
Hereditas|January 1, 1972
Origin of triploidy in human abortusesJ Jonasson, A J Therkelsen, J G Lauritsen, et al.
Pageof 14

Showing results (61-70 of 131) with videos related to

Sort By:
Pageof 14
Experientia|September 15, 1978
Iron malabsorption and hypochromic anemia in a case of Turner's syndromeT Miale, L Stenke, J Lindsten, et al.
Experimental Cell Research|November 1, 1970
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysisT Caspersson, G Gahrton, J Lindsten, et al.
Cancer Detection and Prevention|January 1, 1992
Maternal smoking and irradiation during pregnancy as risk factors for child leukemiaM Stjernfeldt, K Berglund, J Lindsten, et al.
Human Genetics|January 1, 1982
Data and theory for a revised chiasma map of manN E Morton, J Lindsten, L Iselius, et al.
Human Genetics|January 1, 1980
The 11q;22q translocation: a European collaborative analysis of 43 casesM Fraccaro, J Lindsten, C E Ford, et al.
Hereditas|January 1, 1978
Protein binding of ampicillin. Path analysis of a twin materialL Iselius, M Ehrnebo, L O Boréus, et al.
Behavior Genetics|March 1, 1973
An explanation of the apparently increased incidence of moderate mental retardation in Turner's syndromeD C Garron, L Molander, B Cronholm, et al.
Lakartidningen|May 10, 1972
[Prenatal diagnosis of genetic diseases]B Kjessler, J Lindsten, R Zetterström, et al.
Lakartidningen|January 22, 1975
[Prenatal diagnosis of anencephalus and spina bifida by determination of alphafetoprotein]B Hellström, J Lindsten, L Marsk, et al.
Hereditas|January 1, 1972
Origin of triploidy in human abortusesJ Jonasson, A J Therkelsen, J G Lauritsen, et al.
Pageof 14