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 (51-60 of 62) with videos related to

Pageof 7
Sort By:
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Current Biology : CB|January 16, 1999
A selective difference between human Y-chromosomal DNA haplotypesM A Jobling, G A Williams, G A Schiebel, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Molecular Psychiatry|January 7, 2015
Identification and functional characterization of rare SHANK2 variants in schizophreniaS Peykov, S Berkel, M Schoen, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Connective Tissue Research|May 25, 2007
Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sourcesM E Bernardo, J A M Emons, M Karperien, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|March 11, 2021
Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm controlS Hoffmann, S Schmitteckert, K Raedecke, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Current Biology : CB|January 16, 1999
A selective difference between human Y-chromosomal DNA haplotypesM A Jobling, G A Williams, G A Schiebel, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Human Molecular Genetics|April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndromeM Clement-Jones, S Schiller, E Rao, et al.
Molecular Psychiatry|January 7, 2015
Identification and functional characterization of rare SHANK2 variants in schizophreniaS Peykov, S Berkel, M Schoen, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2003
Familial growth and skeletal features associated with SHOX haploinsufficiencyC F J Munns, I A Glass, S Flanagan, et al.
Connective Tissue Research|May 25, 2007
Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sourcesM E Bernardo, J A M Emons, M Karperien, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|March 11, 2021
Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm controlS Hoffmann, S Schmitteckert, K Raedecke, et al.
Developmental Genetics|December 8, 1998
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarrayD H Geschwind, J Gregg, K Boone, et al.
Pageof 7