Detalhe da pesquisa
1.
Next-generation sequencing in X-linked intellectual disability.
Eur J Hum Genet
; 23(11): 1513-8, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25649377
2.
A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.
J Neurol Sci
; 347(1-2): 372-4, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25454649
3.
Identification of the interaction domain of the small terminase subunit pUL89 with the large subunit pUL56 of human cytomegalovirus.
Biochemistry
; 45(29): 8855-63, 2006 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-16846228