about
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patientsFurther delineation of the phenotype caused by biallelic variants in the WDR4 gene.Deletion of the transcription factor SOX4 is implicated in syndromic nephroblastoma.IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differencesPADDAS syndrome associated with hair dysplasia caused by a de novo missense variant of PUM1
P50
description
researcher
@en
wetenschapper
@nl
name
Aurelien Trimouille
@en
Aurelien Trimouille
@nl
type
label
Aurelien Trimouille
@en
Aurelien Trimouille
@nl
prefLabel
Aurelien Trimouille
@en
Aurelien Trimouille
@nl
P31
P496
0000-0002-3457-5684