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J Lindsten

Showing results (121-130 of 131) with videos related to

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Nobel Symposium|January 1, 1973
Studies on spontaneous abortionsA J Therkelsen, O M Jensen, J Jonasson, et al.
Annales De Genetique|January 1, 1991
No evidence of mutations in four candidate genes for male sex determination/differentiation in sex-reversed XY females with campomelic dysplasiaC Ebensperger, R J Jäger, U Lattermann, et al.
Human Genetics|January 1, 1982
Correlation between the number of sex chromosomes and the H-Y antigen titerM Fraccaro, A Mayerová, U Wolf, et al.
Lancet (London, England)|August 13, 1977
Chromosome aberrations and sister-chromatid exchange in workers in chemical laboratories and a rotoprinting factory and in children of women laboratory workersF Funes-Cravioto, C Zapata-Gayon, B Kolmodin-Hedman, et al.
Annals of Human Genetics|May 1, 1975
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2M A Mace, J Noades, E B Robson, et al.
Clinical Genetics|August 1, 1986
Segregation analysis of balanced pericentric inversions in pedigree dataS L Sherman, L Iselius, P Gallano, et al.
Human Genetics|January 1, 1983
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesL Iselius, J Lindsten, A Aurias, et al.
Human Genetics. Supplement|January 1, 1981
Incidence of Down's syndrome in Sweden during the years 1968-1977J Lindsten, L Marsk, K Berglund, et al.
Lakartidningen|February 21, 1979
[The retinoblastoma team at Karolinska hospital]E af Trampe, E O Backlund, M Bergström, et al.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Pageof 14

Showing results (121-130 of 131) with videos related to

Sort By:
Pageof 14
Nobel Symposium|January 1, 1973
Studies on spontaneous abortionsA J Therkelsen, O M Jensen, J Jonasson, et al.
Annales De Genetique|January 1, 1991
No evidence of mutations in four candidate genes for male sex determination/differentiation in sex-reversed XY females with campomelic dysplasiaC Ebensperger, R J Jäger, U Lattermann, et al.
Human Genetics|January 1, 1982
Correlation between the number of sex chromosomes and the H-Y antigen titerM Fraccaro, A Mayerová, U Wolf, et al.
Lancet (London, England)|August 13, 1977
Chromosome aberrations and sister-chromatid exchange in workers in chemical laboratories and a rotoprinting factory and in children of women laboratory workersF Funes-Cravioto, C Zapata-Gayon, B Kolmodin-Hedman, et al.
Annals of Human Genetics|May 1, 1975
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2M A Mace, J Noades, E B Robson, et al.
Clinical Genetics|August 1, 1986
Segregation analysis of balanced pericentric inversions in pedigree dataS L Sherman, L Iselius, P Gallano, et al.
Human Genetics|January 1, 1983
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesL Iselius, J Lindsten, A Aurias, et al.
Human Genetics. Supplement|January 1, 1981
Incidence of Down's syndrome in Sweden during the years 1968-1977J Lindsten, L Marsk, K Berglund, et al.
Lakartidningen|February 21, 1979
[The retinoblastoma team at Karolinska hospital]E af Trampe, E O Backlund, M Bergström, et al.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Pageof 14