Clémence Vanlerberghe
0000-0003-3884-2054
4 papers found
Refreshing results…
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
Phenotypic spectrum of TGFB3 disease‐causing variants in a Dutch‐French cohort and first report of a homozygous patient
Genetics of patella hypoplasia/agenesis
Small patella syndrome: New clinical and molecular insights into a consistent phenotype: Letter to the Editor
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