Referral patterns for microarray testing in prenatal diagnosis (Q43435193)

23 November 2017

Referral patterns for microarray testing in prenatal diagnosis. (English)

1 reference

23 November 2017

9

Mordechai Shohat

1 reference

23 November 2017

Lisa G Shaffer

1

1 reference

23 November 2017

Mindy Preston Dabell

2

1 reference

23 November 2017

Jill A Rosenfeld

3

1 reference

23 November 2017

Nicholas J Neill

4

1 reference

23 November 2017

Blake C Ballif

5

1 reference

23 November 2017

Justine Coppinger

6

1 reference

23 November 2017

Noa Rinzler Diwan

7

1 reference

23 November 2017

Karen Chong

8

1 reference

23 November 2017

David Chitayat

10

1 reference

23 November 2017

1 April 2012

1 reference

23 November 2017

1 reference

23 November 2017

32

1 reference

23 November 2017

4

1 reference

23 November 2017

344-350

1 reference

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

23 November 2017

1 reference

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

21 January 2018

1 reference

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

21 January 2018

1 reference

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

21 January 2018

1 reference

Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases

21 January 2018

1 reference

Array comparative genomic hybridization in global developmental delay.

21 January 2018

1 reference

Array comparative genomic hybridization findings in a cohort referred for an autism evaluation.

21 January 2018

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

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

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

Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.

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

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.

21 January 2018

1 reference

Genomic changes detected by array CGH in human embryos with developmental defects

21 January 2018

1 reference

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

21 January 2018

1 reference

Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

21 January 2018

1 reference

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

21 January 2018

1 reference

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

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

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

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

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

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

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

Use of array-based technology in the practice of medical genetics

21 January 2018

1 reference

The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.

21 January 2018

1 reference

Emerging themes and new challenges in defining the role of structural variation in human disease

21 January 2018

1 reference

Evolving applications of microarray analysis in prenatal diagnosis

21 January 2018

1 reference

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

21 January 2018

1 reference

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.3856

1 reference

23 November 2017

1 reference