Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Gesa Schwanitz

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
American Journal of Medical Genetics. Part A|April 5, 2008
Rare interstitial deletion 9q31.2 to q33.1 de novo: longitudinal study in a patient over a period of more than 20 yearsUlrike Gamerdinger, Thomas Eggermann, Regine Schubert, et al.
European Journal of Medical Genetics|June 10, 2006
First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterizationUlrike Gamerdinger, Kristin Bosse, Thomas Eggermann, et al.
American Journal of Medical Genetics|July 13, 2002
Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literatureRegine Schubert, Thomas Eggermann, Cornelia Hofstaetter, et al.
Cardiology in the Young|February 1, 2005
New trends in chromosomal investigation in children with cardiovascular malformationsRuth Schellberg, Gesa Schwanitz, Lutz Grävinghoff, et al.
Journal of Pediatric Genetics|September 15, 2016
Duplication 3q13.11q23: Longitudinal study in a patient over a period of more than 7 years and refinements of the breakpointsThomas Eggermann, Sabrina Spengler, Ulrike Gamerdinger, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1)Susanne Zahn, Antje Ehrbrecht, Kristin Bosse, et al.
European Journal of Medical Genetics|March 23, 2011
Mosaic tetrasomy 14pterq13.1: longitudinal studyGesa Schwanitz, Eckhard Korsch, Ursula Kremens-Korsch, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14qThomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: characterization and evaluation of the aberrationsGesa Schwanitz, Javad Karim Zad Hagh, Isa Abdi Rad, et al.
Archives of Gynecology and Obstetrics|May 17, 2013
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidiesAndreas Roos, Constantin S von Kaisenberg, Thomas Eggermann, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|April 5, 2008
Rare interstitial deletion 9q31.2 to q33.1 de novo: longitudinal study in a patient over a period of more than 20 yearsUlrike Gamerdinger, Thomas Eggermann, Regine Schubert, et al.
European Journal of Medical Genetics|June 10, 2006
First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterizationUlrike Gamerdinger, Kristin Bosse, Thomas Eggermann, et al.
American Journal of Medical Genetics|July 13, 2002
Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literatureRegine Schubert, Thomas Eggermann, Cornelia Hofstaetter, et al.
Cardiology in the Young|February 1, 2005
New trends in chromosomal investigation in children with cardiovascular malformationsRuth Schellberg, Gesa Schwanitz, Lutz Grävinghoff, et al.
Journal of Pediatric Genetics|September 15, 2016
Duplication 3q13.11q23: Longitudinal study in a patient over a period of more than 7 years and refinements of the breakpointsThomas Eggermann, Sabrina Spengler, Ulrike Gamerdinger, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1)Susanne Zahn, Antje Ehrbrecht, Kristin Bosse, et al.
European Journal of Medical Genetics|March 23, 2011
Mosaic tetrasomy 14pterq13.1: longitudinal studyGesa Schwanitz, Eckhard Korsch, Ursula Kremens-Korsch, et al.
American Journal of Medical Genetics. Part A|February 22, 2005
Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14qThomas Eggermann, Ulrike Gamerdinger, Kristin Bosse, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: characterization and evaluation of the aberrationsGesa Schwanitz, Javad Karim Zad Hagh, Isa Abdi Rad, et al.
Archives of Gynecology and Obstetrics|May 17, 2013
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidiesAndreas Roos, Constantin S von Kaisenberg, Thomas Eggermann, et al.
Pageof 2