Johnny Deladoëy

2PUBLICATIONS
1CO-AUTHORS
Neurogenetics
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Publications (2)

|Mar 11, 2022
Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.

Stéphanie Larrivée-Vanier, Martineau Jean-Louis, Fabien Magne

|Jan 28, 2021
Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.

Stéphanie Larrivée-Vanier, Fabien Magne, Elwaseila Hamdoun

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Frequent Collaborators

1 joint publications

Guy Van Vliet