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H von Koskull

Showing results (1-10 of 47) with videos related to

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Acta Cytologica|July 1, 1984
Rapid identification of glial cells in human amniotic fluid with indirect immunofluorescenceH von Koskull
Cytogenetics and Cell Genetics|January 1, 1973
Nonrandom distribution of chromosome breaks in Fanconi's anemiaH Von Koskull, P Aula
Human Genetics|May 19, 1976
Distribution of spontaneous chromosome breaks in human chromosomesP Aula, H von Koskull
Hereditas|January 1, 1977
Distribution of chromosome breaks in measles, Fanconi's anemia and controlsH von Koskull, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]H von Koskull, J Leisti
Humangenetik|January 1, 1974
Inherited (13;14) translocation and reproduction. Report on three familiesH von Koskull, P Aula
Journal of Cellular Physiology|November 1, 1987
Induction of cytokeratin expression in human mesenchymal cellsH von Koskull, I Virtanen
European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in FinlandH von Koskull, R Salonen
Prenatal Diagnosis|February 1, 1995
Fetal erythroblasts from maternal blood identified with 2,3-bisphosphoglycerate (BPG) and in situ hybridization (ISH) using Y-specific probesH Von Koskull, N Gahmberg
Histochemistry and Cell Biology|January 1, 1996
Focal adhesion kinase pp125FAK is associated with both intercellular junctions and matrix adhesion sites in vivoT Tani, H von Koskull, I Virtanen
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Acta Cytologica|July 1, 1984
Rapid identification of glial cells in human amniotic fluid with indirect immunofluorescenceH von Koskull
Cytogenetics and Cell Genetics|January 1, 1973
Nonrandom distribution of chromosome breaks in Fanconi's anemiaH Von Koskull, P Aula
Human Genetics|May 19, 1976
Distribution of spontaneous chromosome breaks in human chromosomesP Aula, H von Koskull
Hereditas|January 1, 1977
Distribution of chromosome breaks in measles, Fanconi's anemia and controlsH von Koskull, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]H von Koskull, J Leisti
Humangenetik|January 1, 1974
Inherited (13;14) translocation and reproduction. Report on three familiesH von Koskull, P Aula
Journal of Cellular Physiology|November 1, 1987
Induction of cytokeratin expression in human mesenchymal cellsH von Koskull, I Virtanen
European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in FinlandH von Koskull, R Salonen
Prenatal Diagnosis|February 1, 1995
Fetal erythroblasts from maternal blood identified with 2,3-bisphosphoglycerate (BPG) and in situ hybridization (ISH) using Y-specific probesH Von Koskull, N Gahmberg
Histochemistry and Cell Biology|January 1, 1996
Focal adhesion kinase pp125FAK is associated with both intercellular junctions and matrix adhesion sites in vivoT Tani, H von Koskull, I Virtanen
Pageof 5