Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
About this item
Full title
Author / Creator
Petrovski, Slavé , Aggarwal, Vimla , Giordano, Jessica L , Stosic, Melissa , Wou, Karen , Bier, Louise , Spiegel, Erica , Brennan, Kelly , Stong, Nicholas , Jobanputra, Vaidehi , Ren, Zhong , Zhu, Xiaolin , Mebane, Caroline , Nahum, Odelia , Wang, Quanli , Kamalakaran, Sitharthan , Malone, Colin , Anyane-Yeboa, Kwame , Miller, Russell , Levy, Brynn , Goldstein, David B and Wapner, Ronald J
Publisher
England: Elsevier Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: Elsevier Ltd
Subjects
More information
Scope and Contents
Contents
Identification of chromosomal aneuploidies and copy number variants that are associated with fetal structural anomalies has substantial value. Although whole-exome sequencing (WES) has been applied to case series of a few selected prenatal cases, its value in routine clinical settings has not been prospectively assessed in a large unselected cohort...
Alternative Titles
Full title
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Authors, Artists and Contributors
Author / Creator
Aggarwal, Vimla
Giordano, Jessica L
Stosic, Melissa
Wou, Karen
Bier, Louise
Spiegel, Erica
Brennan, Kelly
Stong, Nicholas
Jobanputra, Vaidehi
Ren, Zhong
Zhu, Xiaolin
Mebane, Caroline
Nahum, Odelia
Wang, Quanli
Kamalakaran, Sitharthan
Malone, Colin
Anyane-Yeboa, Kwame
Miller, Russell
Levy, Brynn
Goldstein, David B
Wapner, Ronald J
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2179492250
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2179492250
Other Identifiers
ISSN
0140-6736
E-ISSN
1474-547X
DOI
10.1016/S0140-6736(18)32042-7
