KP
Kalinka Popel

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
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
Article scientifique · 2022
The world through their eyes: The perceptions and lived experience among Capetonian young adults with hereditary visual impairment
Article scientifique · 2020

Domaines principaux

Sciences de la vie et biotechnologies1 Sciences de la santé1 Sciences sociales et comportementales1

Statistiques

Consultations8
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