IS
Isabelle Schrauwen

Publications (3)

Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda
Article scientifique · 2025
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
Article scientifique · 2022
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
Article scientifique · 2022

Domaines principaux

Sciences de la santé2 Sciences de la vie et biotechnologies1

Statistiques

Consultations14
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