Orphanet: Molekulare Diagnostik der famili�ren mesenchymalen Dysgenesie des vorderen Augensegments FOXE3 und PITX3 Gen
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Molecular diagnosis of familial ocular anterior segment mesenchymal dysgenesis (FOXE3 and PITX3 genes)

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Last update: November 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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