Wim Wuyts

3PUBLICATIONS
24CO-AUTHORS
NeurogeneticsDisease surveillance
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Publications (3)

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|Jan 21, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?

Thomas Clabout, Laurence Maes, Frederic Acke

|Jul 13, 2021
Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers.

Joséphine Lantoine, Anne Brysse, Vinciane Dideberg

|Feb 17, 2018
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment.

Sebastien P F JanssensdeVarebeke, Guy Van Camp, Nils Peeters

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Frequent Collaborators

1 joint publications

Guy Van Camp

1 joint publications

Joséphine Lantoine

1 joint publications

Anne Brysse

1 joint publications

Vinciane Dideberg

1 joint publications

Kathleen Claes

1 joint publications

Sofie Symoens

1 joint publications

Wim Coucke

1 joint publications

Valérie Benoit

1 joint publications

Sonia Rombout

1 joint publications

Martine De Rycke

Frequent Collaborators

1 joint publications

Guy Van Camp

1 joint publications

Joséphine Lantoine

1 joint publications

Anne Brysse

1 joint publications

Vinciane Dideberg

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