Detalhe da pesquisa
1.
Prevalence of cytogenetic abnormalities and FMR1 gene premutation in a Portuguese population with premature ovarian insufficiency.
Acta Med Port
; 34(9): 580-585, 2021 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33118925
2.
Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene.
Mol Cytogenet
; 8: 21, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25883683
3.
Advances in the genotyping of thrombosis genetic risk factors: clinical and laboratory implications.
Pathophysiol Haemost Thromb
; 32(5-6): 235-40, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-13679648
4.
Clinicobiological, immunophenotypic, and molecular characteristics of monoclonal CD56-/+dim chronic natural killer cell large granular lymphocytosis.
Am J Pathol
; 165(4): 1117-27, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15466379