Mullerian aplasia and hyperandrogenism

WNT4 - mullerian aplasia and hyperandrogenism

This test is available for the following conditions:

• Conditions > Disorders in sex development > Mullerian aplasia and hyperandrogenism

This product is also part of the following panels:

• WES comprehensive preconception carrier test ¹
• WES Disorders/differences of sex development (DSD) / Primary adrenal insufficiency (99.8% *)
• WES Mendelian inherited disorders (99.8% *)
• WES orofacial clefting (99.8% *)
• WES renal disorders (99.8% *)
• WES renal disorders (99.8% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 603490
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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