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

Andreas Tzschach

Showing results (11-20 of 128) with videos related to

Pageof 13
Sort By:
Psychiatry Research. Neuroimaging|June 11, 2016
Chromosome aberration associated with hippocampal impairmentRobert Haussmann, Gisa Meissner, Jennifer Linn, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disabilityLuisa Mackenroth, Karl Hackmann, Barbara Klink, et al.
American Journal of Medical Genetics. Part A|March 23, 2013
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disabilityAnastasia Gazou, Angelika Riess, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literatureAndreas Tzschach, Luitgard M Graul-Neumann, Kateryna Konrat, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
12q24.33 deletion: report of a patient with intellectual disability and review of the literatureMartin Kehrer, Sylke Singer, Ute Grasshoff, et al.
Gene|November 6, 2012
Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletionGerda Neubert, Katja von Au, Katrin Drossel, et al.
Human Genetics|January 19, 2013
Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patientsStella-Amrei Kunde, Nils Rademacher, Andreas Tzschach, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Characterization of interstitial Xp duplications in two families by tiling path array CGHAndreas Tzschach, Wei Chen, Fikret Erdogan, et al.
Clinical Dysmorphology|June 1, 2017
Pierpont syndrome: report of a new patientAnne-Karin Kahlert, Sabine Weidensee, Luisa Mackenroth, et al.
Ophthalmic Genetics|July 31, 2018
Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletionJanine Lenk, Joseph Porrmann, Martin Smitka, et al.
Pageof 13

Showing results (11-20 of 128) with videos related to

Sort By:
Pageof 13
Psychiatry Research. Neuroimaging|June 11, 2016
Chromosome aberration associated with hippocampal impairmentRobert Haussmann, Gisa Meissner, Jennifer Linn, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disabilityLuisa Mackenroth, Karl Hackmann, Barbara Klink, et al.
American Journal of Medical Genetics. Part A|March 23, 2013
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disabilityAnastasia Gazou, Angelika Riess, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literatureAndreas Tzschach, Luitgard M Graul-Neumann, Kateryna Konrat, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
12q24.33 deletion: report of a patient with intellectual disability and review of the literatureMartin Kehrer, Sylke Singer, Ute Grasshoff, et al.
Gene|November 6, 2012
Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletionGerda Neubert, Katja von Au, Katrin Drossel, et al.
Human Genetics|January 19, 2013
Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patientsStella-Amrei Kunde, Nils Rademacher, Andreas Tzschach, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Characterization of interstitial Xp duplications in two families by tiling path array CGHAndreas Tzschach, Wei Chen, Fikret Erdogan, et al.
Clinical Dysmorphology|June 1, 2017
Pierpont syndrome: report of a new patientAnne-Karin Kahlert, Sabine Weidensee, Luisa Mackenroth, et al.
Ophthalmic Genetics|July 31, 2018
Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletionJanine Lenk, Joseph Porrmann, Martin Smitka, et al.
Pageof 13