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Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.Infectious and immunologic phenotype of MECP2 duplication syndrome.Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia.
P50
description
researcher
@en
wetenschapper
@nl
name
Olivier Patat
@en
Olivier Patat
@nl
type
label
Olivier Patat
@en
Olivier Patat
@nl
prefLabel
Olivier Patat
@en
Olivier Patat
@nl
P31
P496
0000-0001-5759-1540