Detalhe da pesquisa
1.
Contemporary Trends in Cardiac Surgical Care for Trisomy 13 and 18 Patients Admitted to Hospitals in the United States.
J Pediatr
; 268: 113955, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38340889
2.
Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results.
Prenat Diagn
; 44(4): 401-408, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38141050
3.
"She was finally mine": the moral experience of families in the context of trisomy 13 and 18- a scoping review with thematic analysis.
BMC Med Ethics
; 25(1): 24, 2024 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38431625
4.
[Prenatal diagnosis and outcome of pregnancy for women with high risks by screening of fetal free DNA from peripheral blood samples].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(1): 1-7, 2024 Jan 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-38171551
5.
The predictive value of prenatal cell-free DNA testing for rare autosomal trisomies: a systematic review and meta-analysis.
Am J Obstet Gynecol
; 228(3): 292-305.e6, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36027954
6.
Cell-free DNA screening for trisomy 21 in twin pregnancy: a large multicenter cohort study.
Am J Obstet Gynecol
; 229(4): 435.e1-435.e7, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37030426
7.
The common trisomy syndromes, their cardiac implications, and ethical considerations in care.
Curr Opin Pediatr
; 35(5): 531-537, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37551160
8.
Late first-trimester ultrasound findings can alter management after high-risk NIPT result.
Ultrasound Obstet Gynecol
; 62(4): 497-503, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37247395
9.
Association between low fetal fraction in cell-free DNA screening and fetal chromosomal aberrations: A systematic review and meta-analysis.
Prenat Diagn
; 43(7): 838-853, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37143173
10.
Syndromic congenital diaphragmatic hernia: Current incidence and outcome. Analysis from the congenital diaphragmatic hernia study group registry.
Prenat Diagn
; 43(10): 1265-1273, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37418285
11.
Screen-positive rate in cell free DNA screening for trisomy 21.
Prenat Diagn
; 43(12): 1536-1543, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37789581
12.
Non-invasive prenatal testing (NIPT) in twin pregnancies affected by early single fetal demise: A systematic review of NIPT and vanishing twins.
Prenat Diagn
; 43(7): 829-837, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37226326
13.
Prenatal and fetal diagnosis of trisomy 18 after low-risk cell-free fetal DNA screening: A report of four cases.
Prenat Diagn
; 43(1): 36-41, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36426655
14.
Non-Invasive prenatal testing with rolling circle amplification: Real-world clinical experience in a non-molecular laboratory.
J Clin Lab Anal
; 37(6): e24870, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36972484
15.
Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21.
J Assist Reprod Genet
; 40(4): 803-810, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36763299
16.
Trisomies Reorganize Human 3D Genome.
Int J Mol Sci
; 24(22)2023 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38003233
17.
Neck Extension and Intraocular Pressure Elevation During Palatoplasty in a Patient with Patau Syndrome and Congenital Glaucoma: A Case Report.
Cleft Palate Craniofac J
; 60(10): 1326-1330, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35473400
18.
[Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(8): 922-927, 2023 Aug 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-37532489
19.
[Retrospective analysis of cell-free fetal DNA prenatal testing of maternal peripheral blood].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(8): 933-938, 2023 Aug 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-37532491
20.
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Am J Hum Genet
; 105(6): 1091-1101, 2019 12 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31708118