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Acta Cytologica
|
July 1, 1984
Rapid identification of glial cells in human amniotic fluid with indirect immunofluorescence
H von Koskull
Cytogenetics and Cell Genetics
|
January 1, 1973
Nonrandom distribution of chromosome breaks in Fanconi's anemia
H Von Koskull, P Aula
Human Genetics
|
May 19, 1976
Distribution of spontaneous chromosome breaks in human chromosomes
P Aula, H von Koskull
Hereditas
|
January 1, 1977
Distribution of chromosome breaks in measles, Fanconi's anemia and controls
H 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 families
H von Koskull, P Aula
Journal of Cellular Physiology
|
November 1, 1987
Induction of cytokeratin expression in human mesenchymal cells
H von Koskull, I Virtanen
European Journal of Human Genetics : EJHG
|
January 1, 1997
Genetic services in Finland
H 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 probes
H 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 vivo
T Tani, H von Koskull, I Virtanen
Page
of 5
Search research articles
Search
Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Acta Cytologica
|
July 1, 1984
Rapid identification of glial cells in human amniotic fluid with indirect immunofluorescence
H von Koskull
Cytogenetics and Cell Genetics
|
January 1, 1973
Nonrandom distribution of chromosome breaks in Fanconi's anemia
H Von Koskull, P Aula
Human Genetics
|
May 19, 1976
Distribution of spontaneous chromosome breaks in human chromosomes
P Aula, H von Koskull
Hereditas
|
January 1, 1977
Distribution of chromosome breaks in measles, Fanconi's anemia and controls
H 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 families
H von Koskull, P Aula
Journal of Cellular Physiology
|
November 1, 1987
Induction of cytokeratin expression in human mesenchymal cells
H von Koskull, I Virtanen
European Journal of Human Genetics : EJHG
|
January 1, 1997
Genetic services in Finland
H 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 probes
H 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 vivo
T Tani, H von Koskull, I Virtanen
Page
of 5