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Items: 1 to 20 of 274

1.

Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, X, and Y using segmental duplication quantitative fluorescent PCR (SD-QF-PCR).

Sun L, Fan Z, Long J, Weng X, Tang W, Pang W.

Gene. 2017 Sep 5;627:72-78. doi: 10.1016/j.gene.2017.06.014. Epub 2017 Jun 9.

PMID:
28603073
2.

Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS).

Strom CM, Anderson B, Tsao D, Zhang K, Liu Y, Livingston K, Elzinga C, Evans M, Nguyen Q, Wolfson D, Rowland C, Kolacki P, Maxwell M, Wang JC, Rabin D, Catanese J, Owen R, Braastad C, Sun W.

PLoS One. 2017 Mar 1;12(3):e0167130. doi: 10.1371/journal.pone.0167130. eCollection 2017.

3.

Using Patient-Centered Care After a Prenatal Diagnosis of Trisomy 18 or Trisomy 13: A Review.

Haug S, Goldstein M, Cummins D, Fayard E, Merritt TA.

JAMA Pediatr. 2017 Apr 1;171(4):382-387. doi: 10.1001/jamapediatrics.2016.4798. Review.

PMID:
28192554
4.

Cell-free DNA screening in clinical practice: abnormal autosomal aneuploidy and microdeletion results.

Valderramos SG, Rao RR, Scibetta EW, Silverman NS, Han CS, Platt LD.

Am J Obstet Gynecol. 2016 Nov;215(5):626.e1-626.e10. doi: 10.1016/j.ajog.2016.06.039. Epub 2016 Jun 28.

PMID:
27371353
5.

Prenatal diagnosis of trisomy 21, 18 and 13 by quantitative pyrosequencing of segmental duplications.

Tong H, Jin Y, Xu Y, Zou B, Ye H, Wu H, Kumar S, Pitman JL, Zhou G, Song Q.

Clin Genet. 2016 Nov;90(5):451-455. doi: 10.1111/cge.12772. Epub 2016 Apr 8.

PMID:
26948280
6.

Microarray-Based Analysis of Methylation of 1st Trimester Trisomic Placentas from Down Syndrome, Edwards Syndrome and Patau Syndrome.

Hatt L, Aagaard MM, Bach C, Graakjaer J, Sommer S, Agerholm IE, Kølvraa S, Bojesen A.

PLoS One. 2016 Aug 4;11(8):e0160319. doi: 10.1371/journal.pone.0160319. eCollection 2016.

7.

Survival and Surgical Interventions for Children With Trisomy 13 and 18.

Nelson KE, Rosella LC, Mahant S, Guttmann A.

JAMA. 2016 Jul 26;316(4):420-8. doi: 10.1001/jama.2016.9819. Erratum in: JAMA. 2017 May 2;317(17 ):1803.

PMID:
27458947
8.

Trisomy 13 and 18--Treatment Decisions in a Stable Gray Zone.

Lantos JD.

JAMA. 2016 Jul 26;316(4):396-8. doi: 10.1001/jama.2016.9470. No abstract available.

PMID:
27458943
9.

A multicenter study of fetal chromosomal abnormalities in Chinese women of advanced maternal age.

Zhu Y, Lu S, Bian X, Wang H, Zhu B, Wang H, Xu Z, Xu L, Yan W, Zeng Y, Chen Z, Tang S, Shen G, Miao Z.

Taiwan J Obstet Gynecol. 2016 Jun;55(3):379-84. doi: 10.1016/j.tjog.2016.01.002.

10.

Management Considerations for Ongoing Pregnancies Complicated by Trisomy 13 and 18.

Dotters-Katz SK, Kuller JA, Grace MR, Laifer SA, Strauss RA.

Obstet Gynecol Surv. 2016 May;71(5):295-300. doi: 10.1097/OGX.0000000000000304. Review.

PMID:
27182826
11.

Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.

Koumbaris G, Kypri E, Tsangaras K, Achilleos A, Mina P, Neofytou M, Velissariou V, Christopoulou G, Kallikas I, González-Liñán A, Benusiene E, Latos-Bielenska A, Marek P, Santana A, Nagy N, Széll M, Laudanski P, Papageorgiou EA, Ioannides M, Patsalis PC.

Clin Chem. 2016 Jun;62(6):848-55. doi: 10.1373/clinchem.2015.252502. Epub 2016 Apr 26.

12.

Open source non-invasive prenatal testing platform and its performance in a public health laboratory.

Johansen P, Richter SR, Balslev-Harder M, Miltoft CB, Tabor A, Duno M, Kjaergaard S.

Prenat Diagn. 2016 Jun;36(6):530-6. doi: 10.1002/pd.4819. Epub 2016 Apr 24.

PMID:
27027563
13.

Long-term survival of full trisomy 13 in a 14 year old male: a case report.

Imataka G, Hagisawa S, Nitta A, Hirabayashi H, Suzumura H, Arisaka O.

Eur Rev Med Pharmacol Sci. 2016 Mar;20(5):919-22.

14.

Does medical intervention affect outcome in infants with trisomy 18 or trisomy 13?

Kosho T, Carey JC.

Am J Med Genet A. 2016 Apr;170A(4):847-9. doi: 10.1002/ajmg.a.37610. Epub 2016 Mar 8. No abstract available.

PMID:
26955783
15.

Love and the Value of Life in Health Care: A Narrative Medicine Case Study in Medical Education.

Pentiado JA Jr, De Almeida HO, Amorim FF, Facioli AM, Trindade EM, De Almeida KJ.

Perm J. Spring 2016;20(2):98-102. doi: 10.7812/TPP/15-067. Epub 2016 Feb 15.

16.

Trisomy 13: Changing Perspectives.

Macias G, Riley C.

Neonatal Netw. 2016;35(1):31-6. doi: 10.1891/0730-0832.35.1.31.

PMID:
26842537
17.

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.

Taylor-Phillips S, Freeman K, Geppert J, Agbebiyi A, Uthman OA, Madan J, Clarke A, Quenby S, Clarke A.

BMJ Open. 2016 Jan 18;6(1):e010002. doi: 10.1136/bmjopen-2015-010002. Review.

18.

Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.

Pan M, Han J, Zhen L, Yang X, Li R, Liao C, Li DZ.

Eur J Obstet Gynecol Reprod Biol. 2016 Feb;197:164-7. doi: 10.1016/j.ejogrb.2015.12.024. Epub 2015 Dec 30.

PMID:
26771907
19.

Medical and Ethical Considerations Related to Viable Fetuses with Trisomy 13 in the 36th Week of Pregnancy--a Review of the Literature.

Pawelec M, Dżugalik M, Pietras J, Bełza Ł, Latkowski Ł.

Adv Clin Exp Med. 2015 Sep-Oct;24(5):911-21. doi: 10.17219/acem/26324. Review.

20.

Cell-free DNA testing in the maternal blood in high-risk pregnancies after first-trimester combined screening.

Persico N, Boito S, Ischia B, Cordisco A, De Robertis V, Fabietti I, Periti E, Volpe P, Fedele L, Rembouskos G.

Prenat Diagn. 2016 Mar;36(3):232-6. doi: 10.1002/pd.4773. Epub 2016 Feb 9.

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