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B Eiben

Showing results (41-50 of 68) with videos related to

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Prenatal Diagnosis|March 4, 1998
Discordant karyotypes in CVS and amniocenteses using cytogenetic and fluorescence in situ hybridization (FISH) analysesB Eiben, W Trawicki, A Haupt, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|August 14, 2012
Comparison of three first trimester screening algorithms for trisomy 21 with and without adjustment for maternal characteristicsK Lüthgens, E Merz, B J Hackelöer, et al.
Human Genetics|February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunctionT Eggermann, M M Nöthen, B Eiben, et al.
Human Genetics|October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)M M Nöthen, T Eggermann, J Erdmann, et al.
Ultrasound International Open|October 1, 2016
Single Nucleotide Polymorphism-Based Analysis of Cell-Free Fetal DNA in 3000 Cases from Germany and AustriaB Eiben, M Krapp, H Borth, et al.
Current Opinion in Biotechnology|April 21, 2017
Leveraging microbial biosynthetic pathways for the generation of 'drop-in' biofuelsAmin Zargar, Constance B Bailey, Robert W Haushalter, et al.
General & Diagnostic Pathology|January 27, 1998
Villous cytotrophoblast proliferating potential in complete and partial hydatidiform mole: diagnostic value of silver-stained nucleolar organizer region (AgNOR)-associated proteinsH Neudeck, M Unger, P Hufnagl, et al.
Der Gynakologe|June 1, 1988
[Cytogenetic studies of chorionic villi tissue of abortion samples]J Bernert, R Rauskolb, V Jovanovic, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|April 5, 2022
The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester ScreeningE Merz, Ch Thode, B J Hackelöer, et al.
Fetal Diagnosis and Therapy|May 1, 1997
On the complication risk of early amniocentesis versus standard amniocentesisB Eiben, W Hammans, S Hansen, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|March 4, 1998
Discordant karyotypes in CVS and amniocenteses using cytogenetic and fluorescence in situ hybridization (FISH) analysesB Eiben, W Trawicki, A Haupt, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|August 14, 2012
Comparison of three first trimester screening algorithms for trisomy 21 with and without adjustment for maternal characteristicsK Lüthgens, E Merz, B J Hackelöer, et al.
Human Genetics|February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunctionT Eggermann, M M Nöthen, B Eiben, et al.
Human Genetics|October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)M M Nöthen, T Eggermann, J Erdmann, et al.
Ultrasound International Open|October 1, 2016
Single Nucleotide Polymorphism-Based Analysis of Cell-Free Fetal DNA in 3000 Cases from Germany and AustriaB Eiben, M Krapp, H Borth, et al.
Current Opinion in Biotechnology|April 21, 2017
Leveraging microbial biosynthetic pathways for the generation of 'drop-in' biofuelsAmin Zargar, Constance B Bailey, Robert W Haushalter, et al.
General & Diagnostic Pathology|January 27, 1998
Villous cytotrophoblast proliferating potential in complete and partial hydatidiform mole: diagnostic value of silver-stained nucleolar organizer region (AgNOR)-associated proteinsH Neudeck, M Unger, P Hufnagl, et al.
Der Gynakologe|June 1, 1988
[Cytogenetic studies of chorionic villi tissue of abortion samples]J Bernert, R Rauskolb, V Jovanovic, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|April 5, 2022
The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester ScreeningE Merz, Ch Thode, B J Hackelöer, et al.
Fetal Diagnosis and Therapy|May 1, 1997
On the complication risk of early amniocentesis versus standard amniocentesisB Eiben, W Hammans, S Hansen, et al.
Pageof 7