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

B Albrecht

Showing results (101-110 of 112) with videos related to

Pageof 12
Sort By:
Balkan Journal of Medical Genetics : BJMG|November 23, 2013
Human Ring Chromosomes - New Insights for their Clinical SignificanceRs Guilherme, E Klein, Ab Hamid, et al.
European Child & Adolescent Psychiatry|January 6, 2019
Slow cortical potentials neurofeedback in children with ADHD: comorbidity, self-regulation and clinical outcomes 6 months after treatment in a multicenter randomized controlled trialPascal-M Aggensteiner, D Brandeis, S Millenet, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|August 1, 2009
Heterogeneous interleukin-15 inducibilities in murine B16 melanoma and RM-1 prostate carcinoma by interferon-alpha treatmentTzu G Wu, Joana R Perdigão, Theresa K Umhoefer, et al.
Journal of Medical Genetics|May 2, 2006
Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndromeW Seifert, M Holder-Espinasse, S Spranger, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|April 2, 2022
Effect of cilobradine in cats with a first episode of congestive heart failure due to primary cardiomyopathyS C Riesen, E Bomassi, A Bracke, et al.
Human Genetics|April 10, 2013
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndromeJ C Czeschik, C Voigt, Y Alanay, et al.
Human Genetics|November 17, 2016
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autismNuria C Bramswig, H-J Lüdecke, M Pettersson, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicismG Karadima, M Bugge, P Nicolaidis, et al.
Clinical Genetics|November 29, 2007
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeA L Schulz, B Albrecht, C Arici, et al.
Human Mutation|October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified familiesB L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
Balkan Journal of Medical Genetics : BJMG|November 23, 2013
Human Ring Chromosomes - New Insights for their Clinical SignificanceRs Guilherme, E Klein, Ab Hamid, et al.
European Child & Adolescent Psychiatry|January 6, 2019
Slow cortical potentials neurofeedback in children with ADHD: comorbidity, self-regulation and clinical outcomes 6 months after treatment in a multicenter randomized controlled trialPascal-M Aggensteiner, D Brandeis, S Millenet, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|August 1, 2009
Heterogeneous interleukin-15 inducibilities in murine B16 melanoma and RM-1 prostate carcinoma by interferon-alpha treatmentTzu G Wu, Joana R Perdigão, Theresa K Umhoefer, et al.
Journal of Medical Genetics|May 2, 2006
Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndromeW Seifert, M Holder-Espinasse, S Spranger, et al.
Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology|April 2, 2022
Effect of cilobradine in cats with a first episode of congestive heart failure due to primary cardiomyopathyS C Riesen, E Bomassi, A Bracke, et al.
Human Genetics|April 10, 2013
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndromeJ C Czeschik, C Voigt, Y Alanay, et al.
Human Genetics|November 17, 2016
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autismNuria C Bramswig, H-J Lüdecke, M Pettersson, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicismG Karadima, M Bugge, P Nicolaidis, et al.
Clinical Genetics|November 29, 2007
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeA L Schulz, B Albrecht, C Arici, et al.
Human Mutation|October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified familiesB L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
Pageof 12