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Diagnosis of Central Hypothyroidism (gene panel)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 13/06/2017
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Last update: June 2017

Purpose(s)

Post-natal diagnosis
Pre-symptomatic diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

Additional information

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.