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A Rappold

Showing results (81-90 of 160) with videos related to

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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 Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
American Journal of Human Genetics|April 1, 1993
Pseudoautosomal marker DXYS20 and manic depressionM M Nöthen, S Cichon, J Erdmann, 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.
Genes|December 24, 2021
Identification of ZBTB26 as a Novel Risk Factor for Congenital HypothyroidismPhilipp Vick, Birgit Eberle, Daniela Choukair, 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.
Pageof 16

Showing results (81-90 of 160) with videos related to

Sort By:
Pageof 16
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 Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
American Journal of Human Genetics|April 1, 1993
Pseudoautosomal marker DXYS20 and manic depressionM M Nöthen, S Cichon, J Erdmann, 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.
Genes|December 24, 2021
Identification of ZBTB26 as a Novel Risk Factor for Congenital HypothyroidismPhilipp Vick, Birgit Eberle, Daniela Choukair, 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.
Pageof 16