483 related articles for article (PubMed ID: 26253094)
1. Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
van den Veyver IB; Eng CM
Cold Spring Harb Perspect Med; 2015 Aug; 5(10):. PubMed ID: 26253094
[TBL] [Abstract][Full Text] [Related]
2. Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.
Smith LD; Willig LK; Kingsmore SF
Cold Spring Harb Perspect Med; 2015 Dec; 6(2):a023168. PubMed ID: 26684335
[TBL] [Abstract][Full Text] [Related]
3. The current and future impact of genome-wide sequencing on fetal precision medicine.
Sabbagh R; Van den Veyver IB
Hum Genet; 2020 Sep; 139(9):1121-1130. PubMed ID: 31754893
[TBL] [Abstract][Full Text] [Related]
4. [Ways to improve prenatal diagnosis of chromosome abnormalities and congenital defects of fetal development].
Bakharev VA; Polesterov IuA; Gavrilova IuV
Akush Ginekol (Mosk); 1990 Jan; (1):16-8. PubMed ID: 1693812
[No Abstract] [Full Text] [Related]
5. Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing.
Hayward J; Chitty LS
Semin Fetal Neonatal Med; 2018 Apr; 23(2):94-101. PubMed ID: 29305293
[TBL] [Abstract][Full Text] [Related]
6. [Medical genetics and the genome].
Gerdes AM; Vogel I
Ugeskr Laeger; 2014 Nov; 176(46):. PubMed ID: 25394930
[TBL] [Abstract][Full Text] [Related]
7. Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
Hegde M; Santani A; Mao R; Ferreira-Gonzalez A; Weck KE; Voelkerding KV
Arch Pathol Lab Med; 2017 Jun; 141(6):798-805. PubMed ID: 28362156
[TBL] [Abstract][Full Text] [Related]
8. Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathways.
Verhoef TI; Hill M; Drury S; Mason S; Jenkins L; Morris S; Chitty LS
Prenat Diagn; 2016 Jul; 36(7):636-42. PubMed ID: 27107169
[TBL] [Abstract][Full Text] [Related]
9. Noninvasive prenatal diagnosis in 2020.
Lo YM
Prenat Diagn; 2010 Jul; 30(7):702-3. PubMed ID: 20572103
[No Abstract] [Full Text] [Related]
10. Ethical and legal aspects of noninvasive prenatal genetic diagnosis.
Dickens BM
Int J Gynaecol Obstet; 2014 Feb; 124(2):181-4. PubMed ID: 24299974
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis: chances, choices.
Roberts SF
J Fla Med Assoc; 1997; 84(6):374-8. PubMed ID: 9379162
[TBL] [Abstract][Full Text] [Related]
12. Changing indications for invasive testing in an era of improved screening.
Norton ME; Rink BD
Semin Perinatol; 2016 Feb; 40(1):56-66. PubMed ID: 26725145
[TBL] [Abstract][Full Text] [Related]
13. Genetic screening and diagnosis.
Lau TK; Leung TN
Curr Opin Obstet Gynecol; 2005 Apr; 17(2):163-9. PubMed ID: 15758610
[TBL] [Abstract][Full Text] [Related]
14. Get ready for the flood of fetal gene screening.
Greely HT
Nature; 2011 Jan; 469(7330):289-91. PubMed ID: 21248817
[No Abstract] [Full Text] [Related]
15. Diagnostic clinical genome and exome sequencing.
Biesecker LG; Green RC
N Engl J Med; 2014 Jun; 370(25):2418-25. PubMed ID: 24941179
[No Abstract] [Full Text] [Related]
16. High-Resolution and Noninvasive Fetal Exome Screening.
Brand H; Whelan CW; Duyzend M; Lemanski J; Salani M; Hao SP; Wong I; Valkanas E; Cusick C; Genetti C; Dobson L; Studwell C; Gianforcaro K; Wilkins-Haug L; Guseh S; Currall B; Gray K; Talkowski ME
N Engl J Med; 2023 Nov; 389(21):2014-2016. PubMed ID: 37991862
[No Abstract] [Full Text] [Related]
17. Reproductive genetics and today's patient options: prenatal diagnosis.
Willner JP
Mt Sinai J Med; 1998 May; 65(3):173-7. PubMed ID: 9615567
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide significance testing of variation from single case exomes.
Wilfert AB; Chao KR; Kaushal M; Jain S; Zöllner S; Adams DR; Conrad DF
Nat Genet; 2016 Dec; 48(12):1455-1461. PubMed ID: 27776118
[TBL] [Abstract][Full Text] [Related]
19. Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
Ferretti L; Mellis R; Chitty LS
Eur J Med Genet; 2019 Aug; 62(8):103663. PubMed ID: 31085342
[TBL] [Abstract][Full Text] [Related]
20. Controversy and debate on clinical genomics sequencing-paper 2: clinical genome-wide sequencing: don't throw out the baby with the bathwater!
Adam S; Friedman JM
J Clin Epidemiol; 2017 Dec; 92():7-10. PubMed ID: 28916491
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]