Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies-Reference-Cited by-同舟云学术

Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies

Published:2019-05 Issue:5 Volume:21 Page:1065-1073
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Quinlan-Jones Elizabeth,Lord Jenny,Williams Denise,Hamilton Sue,Marton Tamas,Eberhardt Ruth Y.,Rinck Gabriele,Prigmore Elena,Keelagher Rebecca,McMullan Dominic J.,Maher Eamonn R.,Hurles Matthew E.,Kilby Mark D.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/s41436-018-0298-8.pdf

Reference31 articles.

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2. Robson SC Chitty LS Ambler G et al. Evaluation of array comparative genomic hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation. Southampton UK NIHR Journals Library 2017; 4:1-103.

3. Van den Veyver IB Eng CM Genome-wide sequencing for prenatal detection of fetal single-gene disorders. Cold Spring Harb Perspect Med 2015; (5): a023077.

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