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

Bibliografiska uppgifter
Huvudupphovsmän:	Regan, R, Smith, K, Crocker, M, Hedman, A, Honey, B, Hurst, J, Taylor, J, Flint, J, Knight, S
Materialtyp:	Conference item
Publicerad:	2005

Liknande verk

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

Microarray technology in healthcare: A cost analysis in idiopathic learning disability
av: Wordsworth, S, et al.
Publicerad: (2006)

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
av: Koolen, D, et al.
Publicerad: (2008)

Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition.
av: Regan, R, et al.
Publicerad: (2006)

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
av: Wordsworth, S, et al.
Publicerad: (2007)

Screening chromosome ends for learning disability - Small chromosomal rearrangements may be behind idiopathic learning disability
av: Knight, S, et al.
Publicerad: (2000)

SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
av: Price, T, et al.
Publicerad: (2005)

Cryptic genomic imbalances in patients with <it>de novo </it>or familial apparently balanced translocations and abnormal phenotype
av: Kanavakis Emanuel, et al.
Publicerad: (2008-07-01)

Microarray comparative genomic hybridization detection of chromosomal imbalances in uterine cervix carcinoma
av: García José, et al.
Publicerad: (2005-07-01)

DOP-PCR products amplified from genomic DNA can be used reliably in whole genome array CGH studie for the detection of delections and duplications in leukaemia
av: Wilson, K, et al.
Publicerad: (2005)

Genomic imbalances defining novel intellectual disability associated loci
av: Fátima Lopes, et al.
Publicerad: (2019-07-01)

Whole genome microarray analysis, from neonatal blood cards
av: Hogan Michael E, et al.
Publicerad: (2009-07-01)

Construction and evaluation of a whole genome microarray of <it>Chlamydomonas reinhardtii</it>
av: Toepel Jörg, et al.
Publicerad: (2011-11-01)

Microarrays for an integrative genomics /
av: 458514 Kohane, Isaac S., et al.
Publicerad: (2003)

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability
av: A. A. Kashevarova, et al.
Publicerad: (2023-03-01)

Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
av: Luiza Emy Dorfman, et al.
Publicerad: (2015-01-01)

Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
av: Luiza Emy Dorfman, et al.
Publicerad: (2015-01-01)

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
av: Kumar Rachana, et al.
Publicerad: (2011-01-01)

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.
av: Price, T, et al.
Publicerad: (2005)

Genetic Determination of a Cryptic Species in the Littoraria Genus With Whole‐Genome Molecular Resolution
av: Jia‐Wei Xu, et al.
Publicerad: (2024-12-01)

Design of whole-genome tiling microarrays for pseudomonas aeruginosa PAO1.
av: Chong, Anna Siew Chyn.
Publicerad: (2010)

Comparison of Whole Genome Amplification Methods for Further Quantitative Analysis with Microarray-based Comparative Genomic Hybridization
av: Yun-Shien Lee, et al.
Publicerad: (2008-03-01)

Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data
av: Chen Dongrong, et al.
Publicerad: (2003-07-01)

Whole genome protein microarrays for serum profiling of immunodominant antigens of Bacillus anthracis
av: Karen Elizabeth Kempsell, et al.
Publicerad: (2015-08-01)

Investigation of the molecular profile of basal cell carcinoma using whole genome microarrays
av: Joyce Helena, et al.
Publicerad: (2006-12-01)

Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy
av: Robert Lesurf, et al.
Publicerad: (2022-03-01)

Identification of genes and genomic islands correlated with high pathogenicity in Streptococcus suis using whole genome tiling microarrays.
av: Xiao Zheng, et al.
Publicerad: (2011-03-01)

Whole genome sequencing unravels cryptic circulation of divergent dengue virus lineages in the rainforest region of Nigeria
av: Bernard Anyebe Onoja, et al.
Publicerad: (2024-12-01)

A flexible whole-genome microarray for transcriptomics in three-spine stickleback (<it>Gasterosteus aculeatus</it>)
av: Primmer Craig R, et al.
Publicerad: (2009-09-01)

Subtelomeric rearrangements and idiopathic mental retardation
av: Regan, R, et al.
Publicerad: (1999)

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.
av: Ballabio, E, et al.
Publicerad: (2011)

Correction: Genome Analysis of Strains Using a Mixed-Genome Microarray.
av: Sjoerd M. Euser, et al.
Publicerad: (2013-01-01)

Screening chromosome ends for learning disability.
av: Knight, S, et al.
Publicerad: (2000)

Differential Gene Expression Analysis of Placentas with Increased Vascular Resistance and Pre-Eclampsia Using Whole-Genome Microarrays
av: M. Centlow, et al.
Publicerad: (2011-01-01)

Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
av: Mitchell Guttman, et al.
Publicerad: (2007-08-01)

Identification of genomic imbalances in oral clefts
av: Elaine Lustosa-Mendes, et al.
Publicerad: (2021-05-01)

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
av: Ariel M Pani, et al.
Publicerad: (2010-08-01)

Comparative Analysis of Romanian and Swiss Bovine Populations Using Whole Genome Sequencing and SNP Microarrays
av: Alexandru Eugeniu Mizeranschi, et al.
Publicerad: (2023-09-01)

High-resolution genotyping via whole genome hybridizations to microarrays containing long oligonucleotide probes.
av: Yan Fu, et al.
Publicerad: (2010-01-01)

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays
av: Gray Joanna, et al.
Publicerad: (2010-11-01)