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

T Thiel

Showing results (81-90 of 143) with videos related to

Pageof 15
Sort By:
Cardiovascular and Interventional Radiology|September 1, 1997
Local intraarterial thrombolysis: in vitro comparison of various infusion cathetersJ J Froelich, M Hoppe, C Freymann, et al.
International Journal of Oncology|August 30, 2011
Genome-wide copy number profiling using a 100K SNP array reveals novel disease-related genes BORIS and TSHZ1 in juvenile angiofibromaBernhard Schick, Silke Wemmert, Vivienne Willnecker, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 20, 2007
Achondrogenesis Type IA (Houston-Harris): a still-unresolved molecular phenotypeThomas Aigner, Tilman Rau, Manuel Niederhagen, et al.
European Journal of Medical Genetics|July 23, 2011
Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrumDiana Zahnleiter, Udo Trautmann, Arif B Ekici, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.
Journal of Computer Assisted Tomography|May 1, 1997
Boeck sarcoidosis of the breast: mammographic, ultrasound, and MR findingsP P Kenzel, J Hadijuana, N Hosten, et al.
American Journal of Medical Genetics. Part A|December 15, 2018
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblingsMoritz Hebebrand, Georgia Vasileiou, Mandy Krumbiegel, et al.
Clinical Genetics|March 17, 2021
Clinical and molecular delineation of spondylocostal dysostosis type 3Sarah Schuhmann, Heiko Koller, Heinrich Sticht, et al.
European Journal of Medical Genetics|December 18, 2020
Early-onset parkinsonism in PPP2R5D-related neurodevelopmental disorderKatalin L M L Hetzelt, Frank Kerling, Cornelia Kraus, et al.
Magnetic Resonance in Medicine|September 25, 2004
Efficient high-frequency body coil for high-field MRIJ T Vaughan, G Adriany, C J Snyder, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Cardiovascular and Interventional Radiology|September 1, 1997
Local intraarterial thrombolysis: in vitro comparison of various infusion cathetersJ J Froelich, M Hoppe, C Freymann, et al.
International Journal of Oncology|August 30, 2011
Genome-wide copy number profiling using a 100K SNP array reveals novel disease-related genes BORIS and TSHZ1 in juvenile angiofibromaBernhard Schick, Silke Wemmert, Vivienne Willnecker, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 20, 2007
Achondrogenesis Type IA (Houston-Harris): a still-unresolved molecular phenotypeThomas Aigner, Tilman Rau, Manuel Niederhagen, et al.
European Journal of Medical Genetics|July 23, 2011
Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrumDiana Zahnleiter, Udo Trautmann, Arif B Ekici, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.
Journal of Computer Assisted Tomography|May 1, 1997
Boeck sarcoidosis of the breast: mammographic, ultrasound, and MR findingsP P Kenzel, J Hadijuana, N Hosten, et al.
American Journal of Medical Genetics. Part A|December 15, 2018
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblingsMoritz Hebebrand, Georgia Vasileiou, Mandy Krumbiegel, et al.
Clinical Genetics|March 17, 2021
Clinical and molecular delineation of spondylocostal dysostosis type 3Sarah Schuhmann, Heiko Koller, Heinrich Sticht, et al.
European Journal of Medical Genetics|December 18, 2020
Early-onset parkinsonism in PPP2R5D-related neurodevelopmental disorderKatalin L M L Hetzelt, Frank Kerling, Cornelia Kraus, et al.
Magnetic Resonance in Medicine|September 25, 2004
Efficient high-frequency body coil for high-field MRIJ T Vaughan, G Adriany, C J Snyder, et al.
Pageof 15