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

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Regan, R, Smith, K, Crocker, M, Hedman, A, Honey, B, Hurst, J, Taylor, J, Flint, J, Knight, S
Μορφή:	Conference item
Έκδοση:	2005

Παρόμοια τεκμήρια

Idiopathic learning disability and genome imbalance.
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Microarray technology in healthcare: A cost analysis in idiopathic learning disability
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Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition.
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Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
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Screening chromosome ends for learning disability - Small chromosomal rearrangements may be behind idiopathic learning disability
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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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Correction: Genome Analysis of Strains Using a Mixed-Genome Microarray.
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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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Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
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