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G A Rappold

Showing results (21-30 of 62) with videos related to

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The EMBO Journal|July 1, 1987
Identification of a testis-specific gene from the mouse t-complex next to a CpG-rich islandG A Rappold, L Stubbs, S Labeit, et al.
Pediatric Endocrinology Reviews : PER|September 6, 2012
New roles of SHOX as regulator of target genesG A Rappold, C Durand, E Decker, et al.
Clinical Genetics|May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal heightS Spranger, S Kirsch, A Mertz, et al.
Human Genetics|January 1, 1984
Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomesG A Rappold, T Cremer, C Cremer, et al.
Human Molecular Genetics|December 26, 2001
The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activatorE Rao, R J Blaschke, A Marchini, et al.
Journal of Medical Genetics|August 3, 2000
FISH deletion mapping defines a single location for the Y chromosome stature gene, GCYS Kirsch, B Weiss, M De Rosa, et al.
Human Molecular Genetics|September 15, 1999
Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primatesB Gläser, D Myrtek, Y Rumpler, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Human Genetics|January 1, 1984
Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probesG A Rappold, T Cremer, H D Hager, et al.
American Journal of Medical Genetics|May 9, 2001
Cytogenetic and molecular characterization of two isodicentric Y chromosomesP Stankiewicz, Z Hélias-Rodzewicz, K Jakubów-Durska, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
The EMBO Journal|July 1, 1987
Identification of a testis-specific gene from the mouse t-complex next to a CpG-rich islandG A Rappold, L Stubbs, S Labeit, et al.
Pediatric Endocrinology Reviews : PER|September 6, 2012
New roles of SHOX as regulator of target genesG A Rappold, C Durand, E Decker, et al.
Clinical Genetics|May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal heightS Spranger, S Kirsch, A Mertz, et al.
Human Genetics|January 1, 1984
Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomesG A Rappold, T Cremer, C Cremer, et al.
Human Molecular Genetics|December 26, 2001
The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activatorE Rao, R J Blaschke, A Marchini, et al.
Journal of Medical Genetics|August 3, 2000
FISH deletion mapping defines a single location for the Y chromosome stature gene, GCYS Kirsch, B Weiss, M De Rosa, et al.
Human Molecular Genetics|September 15, 1999
Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primatesB Gläser, D Myrtek, Y Rumpler, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Human Genetics|January 1, 1984
Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probesG A Rappold, T Cremer, H D Hager, et al.
American Journal of Medical Genetics|May 9, 2001
Cytogenetic and molecular characterization of two isodicentric Y chromosomesP Stankiewicz, Z Hélias-Rodzewicz, K Jakubów-Durska, et al.
Pageof 7