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

G A Rappold

Showing results (31-40 of 62) with videos related to

Pageof 7
Sort By:
Experimental Cell Research|October 21, 1999
The 3D positioning of ANT2 and ANT3 genes within female X chromosome territories correlates with gene activityS Dietzel, K Schiebel, G Little, et al.
Clinical Endocrinology|May 31, 2002
Trisomy of the short stature homeobox-containing gene (SHOX), resulting from a duplication-deletion of the X chromosomeK A Adamson, I Cross, J A Batch, et al.
Molecular Psychiatry|October 1, 2014
Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviourC Bacon, M Schneider, C Le Magueresse, et al.
Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Clinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb developmentR J Blaschke, A P Monaghan, S Schiller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiencyC F J Munns, M Berry, D Vickers, et al.
Pharmacogenetics|August 16, 2001
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorderB Niesler, T Flohr, M M Nöthen, et al.
The EMBO Journal|December 1, 1984
c-myc and immunoglobulin kappa light chain constant genes are on the 8q+ chromosome of three Burkitt lymphoma lines with t(2;8) translocationsG A Rappold, H Hameister, T Cremer, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Experimental Cell Research|October 21, 1999
The 3D positioning of ANT2 and ANT3 genes within female X chromosome territories correlates with gene activityS Dietzel, K Schiebel, G Little, et al.
Clinical Endocrinology|May 31, 2002
Trisomy of the short stature homeobox-containing gene (SHOX), resulting from a duplication-deletion of the X chromosomeK A Adamson, I Cross, J A Batch, et al.
Molecular Psychiatry|October 1, 2014
Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviourC Bacon, M Schneider, C Le Magueresse, et al.
Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Clinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.
Human Genetics|October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosisG Calabrese, R Fischetto, L Stuppia, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb developmentR J Blaschke, A P Monaghan, S Schiller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiencyC F J Munns, M Berry, D Vickers, et al.
Pharmacogenetics|August 16, 2001
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorderB Niesler, T Flohr, M M Nöthen, et al.
The EMBO Journal|December 1, 1984
c-myc and immunoglobulin kappa light chain constant genes are on the 8q+ chromosome of three Burkitt lymphoma lines with t(2;8) translocationsG A Rappold, H Hameister, T Cremer, et al.
Pageof 7