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

U Moog

Showing results (21-30 of 46) with videos related to

Pageof 5
Sort By:
Human Genetics|September 1, 1994
ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case seriesF Toberer, R Happle, R Schneiderbauer, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Rett syndrome in adolescent and adult females: clinical and molecular genetic findingsE Smeets, E Schollen, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)|August 9, 2001
Lateral facial clefts: a case reportC E de Die-Smulders, U Moog, J J Engelen, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
Molecular Syndromology|January 18, 2013
5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual DisabilityW Kleffmann, A M Zink, J A Lee, et al.
New Microbes and New Infections|November 14, 2015
Acute Q fever infection in Thuringia, Germany, after burial of roe deer fawn cadavers (Capreolus capreolus): a case reportB T Schleenvoigt, L D Sprague, K Mertens, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotypeJ J M Engelen, U Moog, J Weber, et al.
Clinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.
Journal of Inherited Metabolic Disease|August 18, 2009
Mental retardation and inborn errors of metabolismA García-Cazorla, N I Wolf, M Serrano, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Human Genetics|September 1, 1994
ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case seriesF Toberer, R Happle, R Schneiderbauer, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Rett syndrome in adolescent and adult females: clinical and molecular genetic findingsE Smeets, E Schollen, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)|August 9, 2001
Lateral facial clefts: a case reportC E de Die-Smulders, U Moog, J J Engelen, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
Molecular Syndromology|January 18, 2013
5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual DisabilityW Kleffmann, A M Zink, J A Lee, et al.
New Microbes and New Infections|November 14, 2015
Acute Q fever infection in Thuringia, Germany, after burial of roe deer fawn cadavers (Capreolus capreolus): a case reportB T Schleenvoigt, L D Sprague, K Mertens, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotypeJ J M Engelen, U Moog, J Weber, et al.
Clinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.
Journal of Inherited Metabolic Disease|August 18, 2009
Mental retardation and inborn errors of metabolismA García-Cazorla, N I Wolf, M Serrano, et al.
Pageof 5