Orphanet: Molekulare Diagnostik der Peters Anomalie CYP1B1, FOXC1, FOXE3, PAX6 und PITX2 Gen

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Molecular diagnosis of Peters anomaly (CYP1B, FOXC1, FOXE3, PAX6, and PITX2 genes)

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Last update: November 2017

Responsible of diagnostic test


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) (5)
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