(Q45337339)

13 December 2017

title

Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience (English)

1 reference

13 December 2017

C Liao

1

1 reference

13 December 2017

F Fu

2

1 reference

13 December 2017

R Li

3

1 reference

13 December 2017

G-E Xie

4

1 reference

13 December 2017

Y-L Zhang

5

1 reference

13 December 2017

J Li

6

1 reference

13 December 2017

D-Z Li

7

1 reference

13 December 2017

publication date

31 October 2013

1 reference

13 December 2017

1 reference

13 December 2017

volume

86

1 reference

13 December 2017

issue

3

1 reference

13 December 2017

page(s)

264-269

1 reference

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

13 December 2017

cites work

1 reference

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

21 January 2018

1 reference

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

21 January 2018

1 reference

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

21 January 2018

1 reference

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

21 January 2018

1 reference

Application of chromosomal microarray in the evaluation of abnormal prenatal findings

21 January 2018

1 reference

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

21 January 2018

1 reference

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

21 January 2018

1 reference

Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

21 January 2018

1 reference

Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery

21 January 2018

1 reference

Chromosomal microarray versus karyotyping for prenatal diagnosis

21 January 2018

1 reference

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

21 January 2018

1 reference

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control

21 January 2018

1 reference

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

21 January 2018

1 reference

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12271

1 reference

13 December 2017

1 reference