The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature-Reference-Cited by-同舟云学术

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature

Published:2013-09-08 Issue:12 Volume:33 Page:1119-1123
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Callaway Jonathan L. A.¹,Shaffer Lisa G.²,Chitty Lyn S.³⁴⁵,Rosenfeld Jill A.⁶,Crolla John A.¹⁷

Affiliation:

1. Wessex Regional Genetics Laboratory Salisbury District Hospital Salisbury UK

2. Paw Print Genetics Genetic Veterinary Sciences, Inc. Spokane WA USA

3. Clinical and Molecular Genetics Unit UCL Institute of Child Health London UK

4. Great Ormond Street NHS Foundation Trust London UK

5. University College London Hospitals NHS Foundation Trust London UK

6. Signature Genomic Laboratories PerkinElmer, Inc. Spokane WA USA

7. Faculty of Medicine, Department of Human Genetics and Genomic Medicine University of Southampton, Southampton General Hospital Southampton UK

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.4209

Reference32 articles.

1. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

2. Diagnostic Genome Profiling in Mental Retardation

3. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

4. The identification of microdeletion syndromes and other chromosome abnormalities: Cytogenetic methods of the past, new technologies for the future

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

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