The importance of copy numbers in genetic diagnostics and research
Copy number variants play a role in many genetic disorders. The fast, accurate and affordable detection of CNVs is essential for clinical genetic testing and research.
MRC Holland develops tools for the detection of DNA copy numbers and methylation patterns associated with disease. Our MLPA® technique is the gold standard in this field, and is used around the world to study hereditary disorders and tumours.
Latest News
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Nov 19, 2021P483 HER gene family: new probemix launched
We are proud to announce the launch of a new MLPA probemix, P483 HER gene family.
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Nov 19, 2021Research highlight: MLPA in combination with FISH for testing of CLL and B-other-ALL
Two recently published studies highlight the role of MLPA in the analysis of haematological neoplasms.
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Nov 19, 2021Holiday closure & shipping information
MRC Holland will be closed from 25 December 2021 until 2 January 2022. Read this article for more information about ordering deadlines and shipping dates surrounding the holiday season.
Come and Meet Us
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Dec 07, 2021 - Online (starts 16:00 CET; UTC+02:00)
Webinar: Get to Know digitalMLPA
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Jan 13, 2022 - Online (starts 16:00 CET; 10:00 AM BRT; 08:00 AM MST))
Virtual Workshop: MLPA Raw Data Evaluation and Troubleshooting
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Jan 27, 2022 - London, United Kingdom
The Festival of Genomics & Biodata
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Mar 31, 2022 - Berlin, Germany
Workshop: "MLPA – Expert in a Day" – Germany