SNP arrays to confirm X-linkage in a family with idiopathic intellectual disability

ABSTRACT: L061 family with idiopathic non-syndromic intellectual disability remained unsolved after targeted screening of ID-related genes, array-CGH and exome sequencing. In order to perform custom tandem repeat screening on the X chromosome by long read single molecule sequencing, X-linkage needed to be confirmed by SNP arrays.

ORGANISM(S): Homo sapiens

SUBMITTER: Alena Zablotskaya 

PROVIDER: E-MTAB-5903 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress