Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases
Authors
Keywords
-
Journal
Molecular Cytogenetics
Volume 4, Issue 1, Pages 12
Publisher
Springer Nature
Online
2011-05-10
DOI
10.1186/1755-8166-4-12
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations
- (2011) Paola Evangelidou et al. Molecular Cytogenetics
- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
- (2010) David T. Miller et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
- (2010) Hansoo Park et al. NATURE GENETICS
- Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance
- (2010) Joo Wook Ahn et al. Molecular Cytogenetics
- Segmental duplications mediate novel, clinically relevant chromosome rearrangements
- (2009) M. Katharine Rudd et al. HUMAN MOLECULAR GENETICS
- Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases
- (2008) Lina Shao et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies
- (2008) Lisa Edelmann et al. Annals of the New York Academy of Sciences
- Clinical Utility of Contemporary Molecular Cytogenetics
- (2008) Bassem A. Bejjani et al. Annual Review of Genomics and Human Genetics
- The array CGH and its clinical applications
- (2008) Marwan Shinawi et al. DRUG DISCOVERY TODAY
- Private inherited microdeletion/microduplications: Implications in clinical practice
- (2008) Maria Antonietta Mencarelli et al. European Journal of Medical Genetics
- Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives
- (2008) Sandra Darilek et al. GENETICS IN MEDICINE
- Novel microdeletion syndromes detected by chromosome microarrays
- (2008) Anne M. Slavotinek HUMAN GENETICS
- Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens
- (2008) Lisa G. Shaffer et al. PRENATAL DIAGNOSIS
- Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing
- (2007) Edgar A. Otto et al. HUMAN MUTATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More