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Molecular diagnosis of Currarino syndrome (MNX1 gene)
Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/11/2017- Praxis für Humangenetik
- Praxis für Humangenetik
- Brünnlbadgasse 15
- 1090 WIEN
- AUSTRIA
- Director of laboratory : Dr Martin GENCIK
- More information
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)
(1)
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.