Detalhe da pesquisa
1.
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
Am J Hum Genet
; 104(1): 94-111, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30609410
2.
Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions.
J Particip Med
; 10(1): e2, 2018 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33052113