Disorders


 

2p16.1-p15 Deletion Syndrome


 

OMIM


Laboratory Test Method Prenatal Carrier *
CGC Genetics - Porto, Portugal• Deletion/duplication analysis
 

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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