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Human Genetics
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February 1, 1990
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction
J S Lee, J Lindsten, M Anvret
Progress in Clinical and Biological Research
|
January 1, 1985
Role of chorion villi biopsy in prenatal diagnosis of genetic disorders
J Lindsten, L Marsk, M Mikkelsen, et al.
Lakartidningen
|
December 28, 1983
[Fetal diagnosis during the first trimester by transcervical aspiration of chorionic villi]
J Lindsten, H Luthman, L Marsk, et al.
Lancet (London, England)
|
January 14, 1978
Duplication of part of chromosome no. 1 in myeloproliferative diseases
G Gahrton, K Friberg, L Zech, et al.
Annales De Genetique
|
June 1, 1971
Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man
T Caspersson, M Hultén, J Lindsten, et al.
Annales De Genetique
|
June 1, 1971
Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son
M Fraccaro, K Hansson, J Lindsten, et al.
Hereditas
|
January 1, 1978
Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblastic leukemia
G Gahrton, K Friberg, J Lindsten, et al.
Acta Anaesthesiologica Scandinavica
|
October 1, 1982
DNA and chromosome alterations in lymphocytes of operating room personnel and in patients before and after inhalation anaesthesia
K Holmberg, B Lambert, J Lindsten, et al.
Clinical Genetics
|
October 1, 1980
Assay of the beta-glucosidase activity with natural labelled and artificial substrates in cultivated skin fibroblasts from homozygotes and heterozygotes with the Norrbottnian type of Gaucher disease
G Håkansson, S Dreborg, J Lindsten, et al.
Experimental Cell Research
|
November 1, 1970
Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis
T Caspersson, M Hultén, J Lindsten, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 131) with videos related to
Sort By:
Page
of 14
Human Genetics
|
February 1, 1990
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction
J S Lee, J Lindsten, M Anvret
Progress in Clinical and Biological Research
|
January 1, 1985
Role of chorion villi biopsy in prenatal diagnosis of genetic disorders
J Lindsten, L Marsk, M Mikkelsen, et al.
Lakartidningen
|
December 28, 1983
[Fetal diagnosis during the first trimester by transcervical aspiration of chorionic villi]
J Lindsten, H Luthman, L Marsk, et al.
Lancet (London, England)
|
January 14, 1978
Duplication of part of chromosome no. 1 in myeloproliferative diseases
G Gahrton, K Friberg, L Zech, et al.
Annales De Genetique
|
June 1, 1971
Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man
T Caspersson, M Hultén, J Lindsten, et al.
Annales De Genetique
|
June 1, 1971
Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son
M Fraccaro, K Hansson, J Lindsten, et al.
Hereditas
|
January 1, 1978
Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblastic leukemia
G Gahrton, K Friberg, J Lindsten, et al.
Acta Anaesthesiologica Scandinavica
|
October 1, 1982
DNA and chromosome alterations in lymphocytes of operating room personnel and in patients before and after inhalation anaesthesia
K Holmberg, B Lambert, J Lindsten, et al.
Clinical Genetics
|
October 1, 1980
Assay of the beta-glucosidase activity with natural labelled and artificial substrates in cultivated skin fibroblasts from homozygotes and heterozygotes with the Norrbottnian type of Gaucher disease
G Håkansson, S Dreborg, J Lindsten, et al.
Experimental Cell Research
|
November 1, 1970
Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis
T Caspersson, M Hultén, J Lindsten, et al.
Page
of 14