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E Schwinger

Showing results (91-100 of 213) with videos related to

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Nature Genetics|August 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Journal of Medical Genetics|September 1, 1994
Mulvihill-Smith syndrome: case report and reviewO Bartsch, K D Tympner, E Schwinger, et al.
Human Genetics|July 1, 1989
Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?H Rehder, W Coerdt, R Eggers, et al.
Catheterization and Cardiovascular Diagnosis|June 1, 1990
Diagnosis of unexpected atrial septal defect by inspired hydrogen appearance time in adult patients referred for cardiac catheterizationM E Schwinger, P A Tunick, E Glassman, et al.
Human Genetics|July 1, 1993
Polyploidies in abortion material decrease with maternal ageM Neuber, H Rehder, C Zuther, et al.
American Journal of Ophthalmology|June 15, 1992
The gene for autosomal dominant familial exudative vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11Y Li, C Fuhrmann, E Schwinger, et al.
American Heart Journal|May 1, 1990
Vegetations on endocardial surfaces struck by regurgitant jets: diagnosis by transesophageal echocardiographyM E Schwinger, P A Tunick, R S Freedberg, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|November 24, 1999
Isolation and characterization of novel CAG repeat containing genes expressed in human brainC Zühlke, R Kiehl, A Johannsmeyer, et al.
American Journal of Medical Genetics|October 1, 1990
Clinical diagnosis of partial duplication 7qO Bartsch, U Kalbe, T K Ngo, et al.
Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, et al.
Pageof 22

Showing results (91-100 of 213) with videos related to

Sort By:
Pageof 22
Nature Genetics|August 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Journal of Medical Genetics|September 1, 1994
Mulvihill-Smith syndrome: case report and reviewO Bartsch, K D Tympner, E Schwinger, et al.
Human Genetics|July 1, 1989
Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?H Rehder, W Coerdt, R Eggers, et al.
Catheterization and Cardiovascular Diagnosis|June 1, 1990
Diagnosis of unexpected atrial septal defect by inspired hydrogen appearance time in adult patients referred for cardiac catheterizationM E Schwinger, P A Tunick, E Glassman, et al.
Human Genetics|July 1, 1993
Polyploidies in abortion material decrease with maternal ageM Neuber, H Rehder, C Zuther, et al.
American Journal of Ophthalmology|June 15, 1992
The gene for autosomal dominant familial exudative vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11Y Li, C Fuhrmann, E Schwinger, et al.
American Heart Journal|May 1, 1990
Vegetations on endocardial surfaces struck by regurgitant jets: diagnosis by transesophageal echocardiographyM E Schwinger, P A Tunick, R S Freedberg, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|November 24, 1999
Isolation and characterization of novel CAG repeat containing genes expressed in human brainC Zühlke, R Kiehl, A Johannsmeyer, et al.
American Journal of Medical Genetics|October 1, 1990
Clinical diagnosis of partial duplication 7qO Bartsch, U Kalbe, T K Ngo, et al.
Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, et al.
Pageof 22