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

S Spranger

Showing results (21-30 of 34) with videos related to

Pageof 4
Sort By:
European Journal of Human Genetics : EJHG|August 2, 2003
SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6C H Zühlke, M Spranger, S Spranger, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
International Journal of Radiation Biology|August 18, 2000
Effects of low dose radiation therapy on adjuvant induced arthritis in ratsG Hildebrandt, J Jahns, M Hindemith, et al.
Cytogenetic and Genome Research|June 29, 2011
De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformationE Bartels, M Draaken, B Kazmierczak, et al.
Heart (British Cardiac Society)|February 16, 2005
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndromeW Heinritz, A Moschik, A Kujat, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Clinical Genetics|May 14, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS featuresJ Sachwitz, R Meyer, G Fekete, et al.
Neurology|January 29, 2003
Somatic mosaicism and variable penetrance in doublecortin-associated migration disordersL Aigner, G Uyanik, S Couillard-Despres, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Nature Genetics|March 4, 2000
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosisV L Ruiz-Perez, S E Ide, T M Strom, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|August 2, 2003
SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6C H Zühlke, M Spranger, S Spranger, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
International Journal of Radiation Biology|August 18, 2000
Effects of low dose radiation therapy on adjuvant induced arthritis in ratsG Hildebrandt, J Jahns, M Hindemith, et al.
Cytogenetic and Genome Research|June 29, 2011
De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformationE Bartels, M Draaken, B Kazmierczak, et al.
Heart (British Cardiac Society)|February 16, 2005
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndromeW Heinritz, A Moschik, A Kujat, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Clinical Genetics|May 14, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS featuresJ Sachwitz, R Meyer, G Fekete, et al.
Neurology|January 29, 2003
Somatic mosaicism and variable penetrance in doublecortin-associated migration disordersL Aigner, G Uyanik, S Couillard-Despres, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Nature Genetics|March 4, 2000
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosisV L Ruiz-Perez, S E Ide, T M Strom, et al.
Pageof 4