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E Schwinger

Showing results (111-120 of 213) with videos related to

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European Journal of Pediatrics|July 1, 1994
Teratogenic effects in a case of maternal treatment for acute myelocytic leukaemia--neonatal and infantile courseA Artlich, J Möller, A Tschakaloff, et al.
Human Genetics|September 16, 1998
Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestorC Zühlke, F Laccone, M Cossée, et al.
American Heart Journal|February 1, 1991
Isolated collapse of left-sided heart chambers in cardiac tamponade: demonstration by two-dimensional echocardiographyB Fusman, M E Schwinger, R Charney, et al.
Andrologia|January 13, 2005
Rational approach to genetic testing of cystic fibrosis (CF) in infertile menK Mennicke, R D Klingenberg, M Bals-Pratsch, et al.
American Heart Journal|February 1, 1993
Acute valvular obstruction from streptococcal endocarditisR Charney, T N Keltz, L Attai, et al.
American Journal of Medical Genetics|March 15, 1996
VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothersU G Froster, S J Wallner, E Reusche, et al.
Human Reproduction (Oxford, England)|February 1, 1996
Results of cytogenetic analysis in men with severe subfertility prior to intracytoplasmic sperm injectionA A Baschat, W Küpker, S al Hasani, et al.
Human Genetics|January 1, 1985
On the significance of true trisomy 20 mosaicism in amniotic fluid cultureM Djalali, P Steinbach, E Schwinger, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|May 1, 1995
Frequency of common cystic fibrosis gene mutations in chronic bronchitis patientsP Entzian, E Müller, A Boysen, et al.
American Journal of Medical Genetics|May 3, 1996
Short stature in a mother and daughter with terminal deletion of Xp22.3E Schwinger, M Kirschstein, M Greiwe, et al.
Pageof 22

Showing results (111-120 of 213) with videos related to

Sort By:
Pageof 22
European Journal of Pediatrics|July 1, 1994
Teratogenic effects in a case of maternal treatment for acute myelocytic leukaemia--neonatal and infantile courseA Artlich, J Möller, A Tschakaloff, et al.
Human Genetics|September 16, 1998
Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestorC Zühlke, F Laccone, M Cossée, et al.
American Heart Journal|February 1, 1991
Isolated collapse of left-sided heart chambers in cardiac tamponade: demonstration by two-dimensional echocardiographyB Fusman, M E Schwinger, R Charney, et al.
Andrologia|January 13, 2005
Rational approach to genetic testing of cystic fibrosis (CF) in infertile menK Mennicke, R D Klingenberg, M Bals-Pratsch, et al.
American Heart Journal|February 1, 1993
Acute valvular obstruction from streptococcal endocarditisR Charney, T N Keltz, L Attai, et al.
American Journal of Medical Genetics|March 15, 1996
VACTERL with hydrocephalus and branchial arch defects: prenatal, clinical, and autopsy findings in two brothersU G Froster, S J Wallner, E Reusche, et al.
Human Reproduction (Oxford, England)|February 1, 1996
Results of cytogenetic analysis in men with severe subfertility prior to intracytoplasmic sperm injectionA A Baschat, W Küpker, S al Hasani, et al.
Human Genetics|January 1, 1985
On the significance of true trisomy 20 mosaicism in amniotic fluid cultureM Djalali, P Steinbach, E Schwinger, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|May 1, 1995
Frequency of common cystic fibrosis gene mutations in chronic bronchitis patientsP Entzian, E Müller, A Boysen, et al.
American Journal of Medical Genetics|May 3, 1996
Short stature in a mother and daughter with terminal deletion of Xp22.3E Schwinger, M Kirschstein, M Greiwe, et al.
Pageof 22