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Arthur Beaudet

Showing results (11-20 of 17) with videos related to

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Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Human Gene Therapy|August 2, 2013
Transgene expression up to 7 years in nonhuman primates following hepatic transduction with helper-dependent adenoviral vectorsNicola Brunetti-Pierri, Thomas Ng, David Iannitti, et al.
Prenatal Diagnosis|October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testingLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
The complex behavioral phenotype of 15q13.3 microdeletion syndromeMark N Ziats, Robin P Goin-Kochel, Leandra N Berry, et al.
Plos Genetics|March 29, 2014
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndromeMichael F Wangler, Claudia Gonzaga-Jauregui, Tomasz Gambin, et al.
Nature Medicine|February 22, 2019
Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNAJinglan Zhang, Jianli Li, Jennifer B Saucier, et al.
Nature Medicine|January 30, 2019
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNAJinglan Zhang, Jianli Li, Jennifer B Saucier, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Prenatal Diagnosis|April 3, 2012
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literatureAmy Breman, Amber N Pursley, Patricia Hixson, et al.
Human Gene Therapy|August 2, 2013
Transgene expression up to 7 years in nonhuman primates following hepatic transduction with helper-dependent adenoviral vectorsNicola Brunetti-Pierri, Thomas Ng, David Iannitti, et al.
Prenatal Diagnosis|October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testingLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
The complex behavioral phenotype of 15q13.3 microdeletion syndromeMark N Ziats, Robin P Goin-Kochel, Leandra N Berry, et al.
Plos Genetics|March 29, 2014
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndromeMichael F Wangler, Claudia Gonzaga-Jauregui, Tomasz Gambin, et al.
Nature Medicine|February 22, 2019
Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNAJinglan Zhang, Jianli Li, Jennifer B Saucier, et al.
Nature Medicine|January 30, 2019
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNAJinglan Zhang, Jianli Li, Jennifer B Saucier, et al.
Pageof 2