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Showing results (71-80 of 90) with videos related to

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Human Molecular Genetics|April 1, 1995
Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease geneJ J Schrick, L F Onuchic, S T Reeders, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 17, 2001
Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategiesO Henegariu, S Artan, J M Greally, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24M S Malo, B J Blanchard, J M Andresen, et al.
American Journal of Human Genetics|April 3, 2001
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humansB K Jordan, M Mohammed, S T Ching, et al.
Chinese Medical Journal|February 1, 1993
Countercurrent immunoelectrophoresis for diagnosis of acute bacterial pneumonia in Chinese childrenY H Yang, Z F Jiang, X N Chen, et al.
Genomics|April 7, 1999
Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNAX Zhang, H Yang, M J Corydon, et al.
American Journal of Medical Genetics|June 22, 2000
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12)C B Cargile, I McIntosh, M V Clough, et al.
Zhonghua Xin Xue Guan Bing Za Zhi|March 11, 2021
[Evaluation of the safety and efficacy of transcatheter aortic valve replacement with domestic prostheses for patients with severely stenotic bicuspid aortic valve]Q Sun, B Wang, C J Zhu, et al.
Genomics|March 15, 1994
Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13R S Wymore, J R Korenberg, K D Kinoshita, et al.
American Journal of Medical Genetics. Part A|February 11, 2009
Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arraysL Dai, U Bellugi, X-N Chen, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|April 1, 1995
Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease geneJ J Schrick, L F Onuchic, S T Reeders, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 17, 2001
Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategiesO Henegariu, S Artan, J M Greally, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24M S Malo, B J Blanchard, J M Andresen, et al.
American Journal of Human Genetics|April 3, 2001
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humansB K Jordan, M Mohammed, S T Ching, et al.
Chinese Medical Journal|February 1, 1993
Countercurrent immunoelectrophoresis for diagnosis of acute bacterial pneumonia in Chinese childrenY H Yang, Z F Jiang, X N Chen, et al.
Genomics|April 7, 1999
Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNAX Zhang, H Yang, M J Corydon, et al.
American Journal of Medical Genetics|June 22, 2000
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12)C B Cargile, I McIntosh, M V Clough, et al.
Zhonghua Xin Xue Guan Bing Za Zhi|March 11, 2021
[Evaluation of the safety and efficacy of transcatheter aortic valve replacement with domestic prostheses for patients with severely stenotic bicuspid aortic valve]Q Sun, B Wang, C J Zhu, et al.
Genomics|March 15, 1994
Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13R S Wymore, J R Korenberg, K D Kinoshita, et al.
American Journal of Medical Genetics. Part A|February 11, 2009
Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arraysL Dai, U Bellugi, X-N Chen, et al.
Pageof 9