Detalhe da pesquisa
1.
Postnatal genetic testing on cord blood for prenatally identified high-probability cases.
Prenat Diagn
; 43(9): 1120-1131, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37036331
2.
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities.
J Genet Couns
; 32(5): 945-956, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37102371
3.
Chromosomal microarray analysis in pregnancy loss: Is it time for a consensus approach?
Prenat Diagn
; 42(12): 1545-1553, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36176068
4.
High-Resolution and Noninvasive Fetal Exome Screening.
N Engl J Med
; 389(21): 2014-2016, 2023 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37991862
5.
Utility of noninvasive genome-wide screening: a prospective cohort of obstetric patients undergoing diagnostic testing.
Genet Med
; 23(7): 1341-1348, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782554
6.
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice.
J Genet Couns
; 30(2): 439-447, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33108040
7.
Rural distribution of human papilloma virus in low- and middle-income countries.
Exp Mol Pathol
; 104(2): 146-150, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29551573
8.
Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network.
Orphanet J Rare Dis
; 16(1): 210, 2021 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33971915