[Genetics in medical studies].
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Curriculum↗
Biomedical subjects
J Lindsten
Publications and source records attributed to J Lindsten.
[Can environmental poisoning produce genetic injuries in man?].
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Chromosome Aberrations↗
An extra C chromosome and various metabolic abnormalities in the bone marrow from a patient with refractory sideroblastic anaemia.
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Anemia, Sideroblastic↗
Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.
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Adult↗
Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.
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Adult↗
Additional G-like chromosome in a malformed boy.
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Aneuploidy↗
Protein-heparin complexes as a cause of artificial enzyme polymorphism.
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Electrophoresis↗
Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son.
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Adult↗
Pathologic lysosomes and increased urinary glycosylceramide excretion in Fabry's disease. Studies on a family with evidence of linkage with the sex-linked blood group Xg.
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Adult↗
Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man.
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Chromatids↗
Absence of brightly fluorescent Y material in XX men.
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Cytogenetics↗
Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings.
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Abnormalities, Multiple↗
Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.
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Abnormalities, Multiple↗
Rapid identification of human chromosomes by TV-techniques.
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Chromosomes↗
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis.
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Chromosomes, Human, 21-22 and Y↗
Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis.
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Adult↗
Fluorescent staining of heteropycnotic chromosome regions in human interphase nuclei.
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Fluorescence↗
Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence.
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Autoradiography↗