Disorders


 

RPGRIP1L-Related Joubert Syndrome


 

OMIM

GeneLocusProtein
RPGRIP1L16q12.2 

Laboratory Test Method Prenatal Carrier *
Aachen, RWTH, Institute of Human Genetics - Aachen, Germany• Linkage analysis
  
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  
InVitae Corporation - San Francisco, CA, USA  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA  

* 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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