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

Horsthemke

Showing results (201-210 of 368) with videos related to

Pageof 37
Sort By:
Human Genetics|January 1, 1985
Identification of a deletion in the low density lipoprotein (LDL) receptor gene in a patient with familial hypercholesterolaemiaB Horsthemke, A M Kessling, M Seed, et al.
BMC Cancer|August 30, 2011
EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylationLisa C Neumann, Andreas Weinhäusel, Stefanie Thomas, et al.
Human Genetics|February 14, 2007
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndromeDagmar Wieczorek, Michael Ludwig, Stefan Boehringer, et al.
Human Genetics|December 1, 1995
Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndromeG Gillessen-Kaesbach, W Robinson, D Lohmann, et al.
Human Molecular Genetics|January 13, 2006
Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrumSven Fischer, Hermann-Josef Lüdecke, Dagmar Wieczorek, et al.
Cancer|November 1, 1990
Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinomaV Greger, P Schirmacher, J Bohl, et al.
American Journal of Human Genetics|June 1, 1997
Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivationC Jones, C Booth, D Rita, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Computer-based recognition of dysmorphic facesHartmut S Loos, Dagmar Wieczorek, Rolf P Würtz, et al.
American Journal of Human Genetics|January 25, 2003
Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defectKarin Buiting, Stephanie Gross, Christina Lich, et al.
European Journal of Biochemistry|March 1, 1984
Subcellular distribution of particle-bound neutral peptidases capable of hydrolyzing gonadoliberin, thyroliberin, enkephalin and substance PB Horsthemke, P Leblanc, C Kordon, et al.
Pageof 37

Showing results (201-210 of 368) with videos related to

Sort By:
Pageof 37
Human Genetics|January 1, 1985
Identification of a deletion in the low density lipoprotein (LDL) receptor gene in a patient with familial hypercholesterolaemiaB Horsthemke, A M Kessling, M Seed, et al.
BMC Cancer|August 30, 2011
EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylationLisa C Neumann, Andreas Weinhäusel, Stefanie Thomas, et al.
Human Genetics|February 14, 2007
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndromeDagmar Wieczorek, Michael Ludwig, Stefan Boehringer, et al.
Human Genetics|December 1, 1995
Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndromeG Gillessen-Kaesbach, W Robinson, D Lohmann, et al.
Human Molecular Genetics|January 13, 2006
Histone acetylation dependent allelic expression imbalance of BAPX1 in patients with the oculo-auriculo-vertebral spectrumSven Fischer, Hermann-Josef Lüdecke, Dagmar Wieczorek, et al.
Cancer|November 1, 1990
Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinomaV Greger, P Schirmacher, J Bohl, et al.
American Journal of Human Genetics|June 1, 1997
Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivationC Jones, C Booth, D Rita, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Computer-based recognition of dysmorphic facesHartmut S Loos, Dagmar Wieczorek, Rolf P Würtz, et al.
American Journal of Human Genetics|January 25, 2003
Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defectKarin Buiting, Stephanie Gross, Christina Lich, et al.
European Journal of Biochemistry|March 1, 1984
Subcellular distribution of particle-bound neutral peptidases capable of hydrolyzing gonadoliberin, thyroliberin, enkephalin and substance PB Horsthemke, P Leblanc, C Kordon, et al.
Pageof 37