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P Aula

Showing results (21-30 of 161) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1980
[Multiple abnormalities]P Aula, J Rapola
Birth Defects Original Article Series|January 1, 1977
A case of deletion of short arm of chromosome 8J Leisti, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|April 27, 2002
[From avoidance of proteins to amino acid transporter gene--a long journey of lysinuric protein intolerance]P Aula, O Simell
British Medical Journal (Clinical Research Ed.)|May 29, 1982
Decrease in gamma-glutamyl transpeptidase activity in early amniotic fluid in fetal trisomy 18 syndromeH Janlanko, P Aula
Annals of Clinical Research|June 1, 1973
Prenatal karyotype analysis in high risk familiesP Aula, O Karjalainen
American Journal of Medical Genetics|October 1, 1987
Prenatal detection of Salla disease based upon increased free sialic acid in amniocytesM Renlund, P Aula
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
Humangenetik|January 1, 1974
Inherited (13;14) translocation and reproduction. Report on three familiesH von Koskull, P Aula
Pageof 17

Showing results (21-30 of 161) with videos related to

Sort By:
Pageof 17
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1980
[Multiple abnormalities]P Aula, J Rapola
Birth Defects Original Article Series|January 1, 1977
A case of deletion of short arm of chromosome 8J Leisti, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|April 27, 2002
[From avoidance of proteins to amino acid transporter gene--a long journey of lysinuric protein intolerance]P Aula, O Simell
British Medical Journal (Clinical Research Ed.)|May 29, 1982
Decrease in gamma-glutamyl transpeptidase activity in early amniotic fluid in fetal trisomy 18 syndromeH Janlanko, P Aula
Annals of Clinical Research|June 1, 1973
Prenatal karyotype analysis in high risk familiesP Aula, O Karjalainen
American Journal of Medical Genetics|October 1, 1987
Prenatal detection of Salla disease based upon increased free sialic acid in amniocytesM Renlund, P Aula
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
Humangenetik|January 1, 1974
Inherited (13;14) translocation and reproduction. Report on three familiesH von Koskull, P Aula
Pageof 17