Disorders


 

Persistent Mullerian Duct Syndrome, Type I


Synonym(s): PMDS, Type I

 

OMIM

GeneLocusProtein
AMH19p13.3Muellerian-inhibiting factor

Laboratory Test Method Prenatal Carrier *
Medgene, MedGene - Bratislava, Slovakia• Sequence analysis of the entire coding region
 
Praxis fuer Humangenetik Wien - Vienna, Austria• Sequence analysis of the entire coding region
 

* 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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