Disorders


 

Familial Schizencephaly, EMX2-Related


 

OMIM

GeneLocusProtein
EMX210q26.11Homeobox protein EMX2

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain  

* 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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