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