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E Tiller

Showing results (21-30 of 60) with videos related to

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Prenatal Diagnosis|September 10, 2014
Women's views and the impact of noninvasive prenatal testing on procedures in a managed care settingGeorge E Tiller, Hilary B Kershberg, John Goff, et al.
Human Genetics|April 1, 1996
A novel (TA)n polymorphism in the hexokinase II gene: application to noninsulin-dependent diabetes mellitus in the Pima IndiansH Ardehali, G E Tiller, R L Printz, et al.
Human Mutation|February 13, 2004
A novel PTPN11 mutation in LEOPARD syndromeE Conti, T Dottorini, A Sarkozy, et al.
The Journal of Biological Chemistry|August 6, 2017
Arginine mutations in antibody complementarity-determining regions display context-dependent affinity/specificity trade-offsKathryn E Tiller, Lijuan Li, Sandeep Kumar, et al.
Pediatrics|January 1, 1987
Infant pneumonitis associated with cytomegalovirus, Chlamydia, Pneumocystis, and Ureaplasma: follow-upD M Brasfield, S Stagno, R J Whitley, et al.
The Journal of Biological Chemistry|January 5, 1999
Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN)M C Zhang, L He, M Giro, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Physical and linkage mapping of the gene for the alpha3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3G E Tiller, M L Warman, Y Gong, et al.
The Journal of Pediatrics|July 1, 1976
Protracted pneumonitis in young infants associated with perinatally acquired cytomegaloviral infectionR J Whitley, D Brasfield, D W Reynolds, et al.
Human Molecular Genetics|October 7, 2017
Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3Pascal Brouillard, Laura Dupont, Raphael Helaers, et al.
JIMD Reports|July 21, 2020
PMM2-CDG caused by uniparental disomy: Case report and literature reviewLaurien Vaes, George E Tiller, Belén Pérez, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|September 10, 2014
Women's views and the impact of noninvasive prenatal testing on procedures in a managed care settingGeorge E Tiller, Hilary B Kershberg, John Goff, et al.
Human Genetics|April 1, 1996
A novel (TA)n polymorphism in the hexokinase II gene: application to noninsulin-dependent diabetes mellitus in the Pima IndiansH Ardehali, G E Tiller, R L Printz, et al.
Human Mutation|February 13, 2004
A novel PTPN11 mutation in LEOPARD syndromeE Conti, T Dottorini, A Sarkozy, et al.
The Journal of Biological Chemistry|August 6, 2017
Arginine mutations in antibody complementarity-determining regions display context-dependent affinity/specificity trade-offsKathryn E Tiller, Lijuan Li, Sandeep Kumar, et al.
Pediatrics|January 1, 1987
Infant pneumonitis associated with cytomegalovirus, Chlamydia, Pneumocystis, and Ureaplasma: follow-upD M Brasfield, S Stagno, R J Whitley, et al.
The Journal of Biological Chemistry|January 5, 1999
Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN)M C Zhang, L He, M Giro, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Physical and linkage mapping of the gene for the alpha3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3G E Tiller, M L Warman, Y Gong, et al.
The Journal of Pediatrics|July 1, 1976
Protracted pneumonitis in young infants associated with perinatally acquired cytomegaloviral infectionR J Whitley, D Brasfield, D W Reynolds, et al.
Human Molecular Genetics|October 7, 2017
Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3Pascal Brouillard, Laura Dupont, Raphael Helaers, et al.
JIMD Reports|July 21, 2020
PMM2-CDG caused by uniparental disomy: Case report and literature reviewLaurien Vaes, George E Tiller, Belén Pérez, et al.
Pageof 6