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Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause

ABSTRACT: Developmental delay/intellectual disability (DD/ID)affects 2% of our population. However, mostpatients are often leftwithout aspecific diagnosis,with thecorresponding consequences for the patientsand their families. The application of microarray technology in the study of patients with DD/ID allows whole-genome analysis with a high resolutionand performance. Here we present the results of a case included in a series of 246 patients with DD/ID, as part of the screening of the genetic causes responsible for their phenotype. SNP-array was performed on Genome-Wide Human SNP_6 (Affymetrix) as recommended by the manufacter. Analysis was performed with Affymetrix reference profile 'GenomeWideSNP_6.hapmap270.na31.r1.a5.ref'.

ORGANISM(S): Homo sapiens

SUBMITTER: Francisco Martinez

PROVIDER: E-GEOD-62438 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause

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Application of CGH-array and SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause

Project description:This SuperSeries is composed of the SubSeries listed below.

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