about
Phenotyping GABA transaminase deficiency: a case description and literature review.Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrationsClinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.Further delineation of the KBG syndrome caused by ANKRD11 aberrations.Woodhouse-Sakati Syndrome: First report of a Portuguese case16q22.1 microdeletion and anticipatory guidance
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-8512-7582
@en
name
Pedro Louro
@ast
Pedro Louro
@en
Pedro Louro
@es
Pedro Louro
@nl
type
label
Pedro Louro
@ast
Pedro Louro
@en
Pedro Louro
@es
Pedro Louro
@nl
prefLabel
Pedro Louro
@ast
Pedro Louro
@en
Pedro Louro
@es
Pedro Louro
@nl
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P21
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P496
0000-0002-8512-7582