Detalhe da pesquisa
1.
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome.
Prenat Diagn
; 43(2): 183-191, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36600414
2.
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.
Prenat Diagn
; 43(2): 192-206, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36726284
3.
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?
J Clin Med
; 11(15)2022 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35956203