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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Regan, R, Smith, K, Crocker, M, Hedman, A, Honey, B, Hurst, J, Taylor, J, Flint, J, Knight, S
التنسيق:	Conference item
منشور في:	2005

مواد مشابهة

Idiopathic learning disability and genome imbalance.
حسب: Knight, S, وآخرون
منشور في: (2006)

Microarray technology in healthcare: A cost analysis in idiopathic learning disability
حسب: Wordsworth, S, وآخرون
منشور في: (2006)

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
حسب: Koolen, D, وآخرون
منشور في: (2008)

Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition.
حسب: Regan, R, وآخرون
منشور في: (2006)

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
حسب: Wordsworth, S, وآخرون
منشور في: (2007)

Screening chromosome ends for learning disability - Small chromosomal rearrangements may be behind idiopathic learning disability
حسب: Knight, S, وآخرون
منشور في: (2000)

SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
حسب: Price, T, وآخرون
منشور في: (2005)

Cryptic genomic imbalances in patients with <it>de novo </it>or familial apparently balanced translocations and abnormal phenotype
حسب: Kanavakis Emanuel, وآخرون
منشور في: (2008-07-01)

Microarray comparative genomic hybridization detection of chromosomal imbalances in uterine cervix carcinoma
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منشور في: (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
حسب: Wilson, K, وآخرون
منشور في: (2005)

Genomic imbalances defining novel intellectual disability associated loci
حسب: Fátima Lopes, وآخرون
منشور في: (2019-07-01)

Whole genome microarray analysis, from neonatal blood cards
حسب: Hogan Michael E, وآخرون
منشور في: (2009-07-01)

Construction and evaluation of a whole genome microarray of <it>Chlamydomonas reinhardtii</it>
حسب: Toepel Jörg, وآخرون
منشور في: (2011-11-01)

Microarrays for an integrative genomics /
حسب: 458514 Kohane, Isaac S., وآخرون
منشور في: (2003)

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability
حسب: A. A. Kashevarova, وآخرون
منشور في: (2023-03-01)

Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
حسب: Luiza Emy Dorfman, وآخرون
منشور في: (2015-01-01)

Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
حسب: Luiza Emy Dorfman, وآخرون
منشور في: (2015-01-01)

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
حسب: Kumar Rachana, وآخرون
منشور في: (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.
حسب: Price, T, وآخرون
منشور في: (2005)

Genetic Determination of a Cryptic Species in the Littoraria Genus With Whole‐Genome Molecular Resolution
حسب: Jia‐Wei Xu, وآخرون
منشور في: (2024-12-01)

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

Comparison of Whole Genome Amplification Methods for Further Quantitative Analysis with Microarray-based Comparative Genomic Hybridization
حسب: Yun-Shien Lee, وآخرون
منشور في: (2008-03-01)

Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data
حسب: Chen Dongrong, وآخرون
منشور في: (2003-07-01)

Whole genome protein microarrays for serum profiling of immunodominant antigens of Bacillus anthracis
حسب: Karen Elizabeth Kempsell, وآخرون
منشور في: (2015-08-01)

Investigation of the molecular profile of basal cell carcinoma using whole genome microarrays
حسب: Joyce Helena, وآخرون
منشور في: (2006-12-01)

Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy
حسب: Robert Lesurf, وآخرون
منشور في: (2022-03-01)

Identification of genes and genomic islands correlated with high pathogenicity in Streptococcus suis using whole genome tiling microarrays.
حسب: Xiao Zheng, وآخرون
منشور في: (2011-03-01)

Whole genome sequencing unravels cryptic circulation of divergent dengue virus lineages in the rainforest region of Nigeria
حسب: Bernard Anyebe Onoja, وآخرون
منشور في: (2024-12-01)

A flexible whole-genome microarray for transcriptomics in three-spine stickleback (<it>Gasterosteus aculeatus</it>)
حسب: Primmer Craig R, وآخرون
منشور في: (2009-09-01)

Subtelomeric rearrangements and idiopathic mental retardation
حسب: Regan, R, وآخرون
منشور في: (1999)

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.
حسب: Ballabio, E, وآخرون
منشور في: (2011)

Correction: Genome Analysis of Strains Using a Mixed-Genome Microarray.
حسب: Sjoerd M. Euser, وآخرون
منشور في: (2013-01-01)

Screening chromosome ends for learning disability.
حسب: Knight, S, وآخرون
منشور في: (2000)

Differential Gene Expression Analysis of Placentas with Increased Vascular Resistance and Pre-Eclampsia Using Whole-Genome Microarrays
حسب: M. Centlow, وآخرون
منشور في: (2011-01-01)

Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
حسب: Mitchell Guttman, وآخرون
منشور في: (2007-08-01)

Identification of genomic imbalances in oral clefts
حسب: Elaine Lustosa-Mendes, وآخرون
منشور في: (2021-05-01)

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
حسب: Ariel M Pani, وآخرون
منشور في: (2010-08-01)

Comparative Analysis of Romanian and Swiss Bovine Populations Using Whole Genome Sequencing and SNP Microarrays
حسب: Alexandru Eugeniu Mizeranschi, وآخرون
منشور في: (2023-09-01)

High-resolution genotyping via whole genome hybridizations to microarrays containing long oligonucleotide probes.
حسب: Yan Fu, وآخرون
منشور في: (2010-01-01)

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays
حسب: Gray Joanna, وآخرون
منشور في: (2010-11-01)