Detalhe da pesquisa
1.
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Am J Hum Genet;
103(5): 786-793, 2018 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30343942
2.
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome.
Am J Med Genet A;
176(4): 862-876, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29460469
3.
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Am J Hum Genet;
103(6): 1054-1055, 2018 12 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30526864