Whole genome microarrays for the detection of cryptic genomic imbalances in idiopathic learning disability

Whole genome microarrays for the detection of cryptic genomic imbalances in idiopathic learning disability

Bibliografiske detaljer
Main Authors:	Regan, R, Smith, K, Crocker, M, Hedman, A, Honey, B, Hurst, J, Taylor, J, Flint, J, Knight, S
Format:	Conference item
Udgivet:	2005

Lignende værker

Idiopathic learning disability and genome imbalance.
af: Knight, S, et al.
Udgivet: (2006)

Microarray technology in healthcare: A cost analysis in idiopathic learning disability
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Udgivet: (2006)

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
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Udgivet: (2008)

Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition.
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Udgivet: (2006)

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
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Udgivet: (2007)

Screening chromosome ends for learning disability - Small chromosomal rearrangements may be behind idiopathic learning disability
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Udgivet: (2000)

SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
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Udgivet: (2005)

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Genomic imbalances defining novel intellectual disability associated loci
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Udgivet: (2019-07-01)

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Construction and evaluation of a whole genome microarray of <it>Chlamydomonas reinhardtii</it>
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Microarrays for an integrative genomics /
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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability
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Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
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Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
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Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
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SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.
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Udgivet: (2005)

Genetic Determination of a Cryptic Species in the Littoraria Genus With Whole‐Genome Molecular Resolution
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Design of whole-genome tiling microarrays for pseudomonas aeruginosa PAO1.
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Comparison of Whole Genome Amplification Methods for Further Quantitative Analysis with Microarray-based Comparative Genomic Hybridization
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Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data
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Whole genome protein microarrays for serum profiling of immunodominant antigens of Bacillus anthracis
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Investigation of the molecular profile of basal cell carcinoma using whole genome microarrays
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Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy
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Identification of genes and genomic islands correlated with high pathogenicity in Streptococcus suis using whole genome tiling microarrays.
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Whole genome sequencing unravels cryptic circulation of divergent dengue virus lineages in the rainforest region of Nigeria
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A flexible whole-genome microarray for transcriptomics in three-spine stickleback (<it>Gasterosteus aculeatus</it>)
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Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.
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Correction: Genome Analysis of Strains Using a Mixed-Genome Microarray.
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Screening chromosome ends for learning disability.
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Differential Gene Expression Analysis of Placentas with Increased Vascular Resistance and Pre-Eclampsia Using Whole-Genome Microarrays
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Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
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Identification of genomic imbalances in oral clefts
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Udgivet: (2021-05-01)

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
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Comparative Analysis of Romanian and Swiss Bovine Populations Using Whole Genome Sequencing and SNP Microarrays
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High-resolution genotyping via whole genome hybridizations to microarrays containing long oligonucleotide probes.
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Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays
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