Catalog

The LCG has different array resolutions in order to identify Copy number variations (CNV) and detection of loss of heterozygosity. This diagnosis can be done on pre-natal and post-natal samples.

EBV based lymphocyte immortalization

MS-MLPA can be used for the analysis of both methylation as well as copy number changes of syndromic related regions.

MLPA can be used for the analysis of copy number changes in DNA of syndromic related regions