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

Heiko Reutter

Showing results (101-110 of 209) with videos related to

Pageof 21
Sort By:
Children (Basel, Switzerland)|December 23, 2023
"Multisystem Inflammatory Syndrome in Children"-Like Disease after COVID-19 Vaccination (MIS-V) with Potential Significance of Functional Active Autoantibodies Targeting G-Protein-Coupled Receptors (GPCR-fAAb) for Pathophysiology and TherapyMarius Schmidt, Steven Hébert, Gerd Wallukat, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Human Mutation|April 5, 2014
Cantú syndrome resulting from activating mutation in the KCNJ8 genePaige E Cooper, Heiko Reutter, Joachim Woelfle, et al.
Frontiers in Pediatrics|August 22, 2025
Development of the EPO-Score - a multivariable tool to predict adverse outcome in infants with perinatal asphyxia undergoing therapeutic hypothermia - a retrospective studyAdriana van der Donk, Maria Schleier, Alisa Bär, et al.
Scientific Reports|October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formationEnrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Isolated cytokine-enriched pericardial effusion: A likely key feature for Aymé-Gripp syndromeAnna-Lina König, Hemmen Sabir, Brigitte Strizek, et al.
Orphanet Journal of Rare Diseases|December 15, 2017
Epidemiologic analysis of families with isolated anorectal malformations suggests high prevalence of autosomal dominant inheritanceGabriel C Dworschak, Nadine Zwink, Eberhard Schmiedeke, et al.
Prenatal Diagnosis|September 3, 2016
Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndromeChristina Kehrer, Alexander Hoischen, Ralf Menkhaus, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 19, 2015
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regionsSophia K Krutzke, Hartmut Engels, Andrea Hofmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 31, 2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian familyHeiko Reutter, Franz Rüschendorf, Manuel Mattheisen, et al.
Pageof 21

Showing results (101-110 of 209) with videos related to

Sort By:
Pageof 21
Children (Basel, Switzerland)|December 23, 2023
"Multisystem Inflammatory Syndrome in Children"-Like Disease after COVID-19 Vaccination (MIS-V) with Potential Significance of Functional Active Autoantibodies Targeting G-Protein-Coupled Receptors (GPCR-fAAb) for Pathophysiology and TherapyMarius Schmidt, Steven Hébert, Gerd Wallukat, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Human Mutation|April 5, 2014
Cantú syndrome resulting from activating mutation in the KCNJ8 genePaige E Cooper, Heiko Reutter, Joachim Woelfle, et al.
Frontiers in Pediatrics|August 22, 2025
Development of the EPO-Score - a multivariable tool to predict adverse outcome in infants with perinatal asphyxia undergoing therapeutic hypothermia - a retrospective studyAdriana van der Donk, Maria Schleier, Alisa Bär, et al.
Scientific Reports|October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formationEnrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Isolated cytokine-enriched pericardial effusion: A likely key feature for Aymé-Gripp syndromeAnna-Lina König, Hemmen Sabir, Brigitte Strizek, et al.
Orphanet Journal of Rare Diseases|December 15, 2017
Epidemiologic analysis of families with isolated anorectal malformations suggests high prevalence of autosomal dominant inheritanceGabriel C Dworschak, Nadine Zwink, Eberhard Schmiedeke, et al.
Prenatal Diagnosis|September 3, 2016
Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndromeChristina Kehrer, Alexander Hoischen, Ralf Menkhaus, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 19, 2015
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regionsSophia K Krutzke, Hartmut Engels, Andrea Hofmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 31, 2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian familyHeiko Reutter, Franz Rüschendorf, Manuel Mattheisen, et al.
Pageof 21