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M Ryynänen

Showing results (1-10 of 109) with videos related to

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Katilolehti|October 1, 1983
[Diagnosing developmental abnormalities by AFP screening]M Ryynänen
Journal of Synchrotron Radiation|July 21, 2004
A magnet model for a hybrid undulator assemblyM Ryynänen
The Journal of Reproductive Medicine|June 1, 1995
First-trimester manifestation of intrahepatic cholestasis of pregnancy and high fetoplacental hormone production in a triploid fetus. A case reportP Kirkinen, M Ryynänen
Genomics|December 1, 1991
D12S17 (YNH15) and D12S25 (CRI-L809) are the same polymorphic locusM Ryynänen, R G Knowlton
Neurosurgery|November 1, 1993
Familial subarachnoid hemorrhage in east Finland, 1977-1990A Ronkainen, J Hernesniemi, M Ryynänen
American Journal of Public Health|April 7, 1999
The effects on fetal development of high alpha-fetoprotein and maternal smokingS Heinonen, M Ryynänen, P Kirkinen
Human Mutation|January 1, 1993
Identification of a leucine-to-proline mutation in the keratin 5 gene in a family with the generalized Köbner type of epidermolysis bullosa simplexW Dong, M Ryynänen, J Uitto
Upsala Journal of Medical Sciences|January 1, 1990
Selecting a sensitive immunoradiometric method of maternal serum alphafetoprotein for prenatal screening of abnormalities in the fetusI M Penttilä, E Puhakainen, M Ryynänen
Acta Obstetricia Et Gynecologica Scandinavica|January 26, 2000
Etiology and outcome of second trimester non-immunologic fetal hydropsS Heinonen, M Ryynänen, P Kirkinen
Journal of Perinatal Medicine|January 1, 1990
Antenatally diagnosed fetal hydronephrosis. Five year's follow upM Ryynänen, A Martikainen, S Saarikoski
Pageof 11

Showing results (1-10 of 109) with videos related to

Sort By:
Pageof 11
Katilolehti|October 1, 1983
[Diagnosing developmental abnormalities by AFP screening]M Ryynänen
Journal of Synchrotron Radiation|July 21, 2004
A magnet model for a hybrid undulator assemblyM Ryynänen
The Journal of Reproductive Medicine|June 1, 1995
First-trimester manifestation of intrahepatic cholestasis of pregnancy and high fetoplacental hormone production in a triploid fetus. A case reportP Kirkinen, M Ryynänen
Genomics|December 1, 1991
D12S17 (YNH15) and D12S25 (CRI-L809) are the same polymorphic locusM Ryynänen, R G Knowlton
Neurosurgery|November 1, 1993
Familial subarachnoid hemorrhage in east Finland, 1977-1990A Ronkainen, J Hernesniemi, M Ryynänen
American Journal of Public Health|April 7, 1999
The effects on fetal development of high alpha-fetoprotein and maternal smokingS Heinonen, M Ryynänen, P Kirkinen
Human Mutation|January 1, 1993
Identification of a leucine-to-proline mutation in the keratin 5 gene in a family with the generalized Köbner type of epidermolysis bullosa simplexW Dong, M Ryynänen, J Uitto
Upsala Journal of Medical Sciences|January 1, 1990
Selecting a sensitive immunoradiometric method of maternal serum alphafetoprotein for prenatal screening of abnormalities in the fetusI M Penttilä, E Puhakainen, M Ryynänen
Acta Obstetricia Et Gynecologica Scandinavica|January 26, 2000
Etiology and outcome of second trimester non-immunologic fetal hydropsS Heinonen, M Ryynänen, P Kirkinen
Journal of Perinatal Medicine|January 1, 1990
Antenatally diagnosed fetal hydronephrosis. Five year's follow upM Ryynänen, A Martikainen, S Saarikoski
Pageof 11