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Items: 1 to 20 of 127

1.

Prenatal Genetic Testing Options.

Jelin AC, Sagaser KG, Wilkins-Haug L.

Pediatr Clin North Am. 2019 Apr;66(2):281-293. doi: 10.1016/j.pcl.2018.12.016. Review.

PMID:
30819336
2.

Prenatal screening for fetal aneuploidy in singleton pregnancies.

Chitayat D, Langlois S, Douglas Wilson R; SOGC GENETICS COMMITTEE; CCMG PRENATAL DIAGNOSIS COMMITTEE.

J Obstet Gynaecol Can. 2011 Jul;33(7):736-750. doi: 10.1016/S1701-2163(16)34961-1.

PMID:
21749752
3.

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. doi: 10.1016/j.siny.2017.12.002. Epub 2018 Jan 2. Review.

PMID:
29305293
4.

Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.

Fonda Allen J, Stoll K, Bernhardt BA.

Semin Perinatol. 2016 Feb;40(1):44-55. doi: 10.1053/j.semperi.2015.11.007. Epub 2015 Dec 21. Review.

5.

Whole Exome Sequencing: Applications in Prenatal Genetics.

Jelin AC, Vora N.

Obstet Gynecol Clin North Am. 2018 Mar;45(1):69-81. doi: 10.1016/j.ogc.2017.10.003. Review.

6.

New genetic testing in prenatal diagnosis.

Babkina N, Graham JM Jr.

Semin Fetal Neonatal Med. 2014 Jun;19(3):214-9. doi: 10.1016/j.siny.2013.10.005. Epub 2013 Dec 4. Review.

PMID:
24315623
7.

Screening for fetal chromosomal and subchromosomal disorders.

Harris S, Reed D, Vora NL.

Semin Fetal Neonatal Med. 2018 Apr;23(2):85-93. doi: 10.1016/j.siny.2017.10.006. Epub 2017 Nov 8. Review.

8.

Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.

Tamminga S, van Maarle M, Henneman L, Oudejans CB, Cornel MC, Sistermans EA.

Adv Clin Chem. 2016;74:63-102. doi: 10.1016/bs.acc.2015.12.004. Epub 2016 Jan 21. Review.

PMID:
27117661
9.

Screening for fetal aneuploidy.

Rink BD, Norton ME.

Semin Perinatol. 2016 Feb;40(1):35-43. doi: 10.1053/j.semperi.2015.11.006. Epub 2015 Dec 25. Review.

PMID:
26725144
10.

Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA.

Chitty LS, Lo YM.

Cold Spring Harb Perspect Med. 2015 Jul 17;5(9):a023085. doi: 10.1101/cshperspect.a023085. Review.

11.

Noninvasive prenatal diagnosis using next-generation sequencing.

Xu L, Shi R.

Gynecol Obstet Invest. 2014;77(2):73-7. doi: 10.1159/000355693. Epub 2013 Oct 26. Review.

PMID:
24192219
12.

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made.

Lench N, Barrett A, Fielding S, McKay F, Hill M, Jenkins L, White H, Chitty LS.

Prenat Diagn. 2013 Jun;33(6):555-62. doi: 10.1002/pd.4124. Review.

PMID:
23592512
13.

Genetic counselling, patient education, and informed decision-making in the genomic era.

Metcalfe SA.

Semin Fetal Neonatal Med. 2018 Apr;23(2):142-149. doi: 10.1016/j.siny.2017.11.010. Epub 2017 Dec 8. Review.

PMID:
29233487
14.

Noninvasive prenatal testing using cell-free fetal DNA in maternal plasma.

Dharajiya N, Zwiefelhofer T, Guan X, Angkachatchai V, Saldivar JS.

Curr Protoc Hum Genet. 2015 Jan 20;84:8.15.1-20. doi: 10.1002/0471142905.hg0815s84. Review.

PMID:
25599670
15.

Prenatal Diagnosis Procedures and Techniques to Obtain a Diagnostic Fetal Specimen or Tissue: Maternal and Fetal Risks and Benefits.

Wilson RD, Gagnon A, Audibert F, Campagnolo C, Carroll J; GENETICS COMMITTEE.

J Obstet Gynaecol Can. 2015 Jul;37(7):656-668. doi: 10.1016/S1701-2163(15)30205-X. English, French.

PMID:
26366824
16.

[New frontiers in noninvasive, prenatal screening and diagnosis: fetal DNA circulating in maternal blood].

Montagnana M, Lippi G, Guidi GC.

Minerva Ginecol. 2007 Jun;59(3):331-41. Review. Italian.

PMID:
17576408
17.

Changing indications for invasive testing in an era of improved screening.

Norton ME, Rink BD.

Semin Perinatol. 2016 Feb;40(1):56-66. doi: 10.1053/j.semperi.2015.11.008. Epub 2015 Dec 24. Review.

PMID:
26725145
18.

Prenatal screening and diagnosis for pediatricians.

Cunniff C; American Academy of Pediatrics Committee on Genetics.

Pediatrics. 2004 Sep;114(3):889-94. Review.

PMID:
15342871
19.

Prenatal screening for and diagnosis of aneuploidy in twin pregnancies.

Audibert F, Gagnon A; Genetics Committee of the Society of Obstetricians and Gynaecologists of Canada; Prenatal Diagnosis Committee of the Canadian College of Medical Geneticists.

J Obstet Gynaecol Can. 2011 Jul;33(7):754-67.

PMID:
21749753
20.

Ethical issues in perinatal genetics.

Chervenak FA, McCullough LB.

Semin Fetal Neonatal Med. 2011 Apr;16(2):70-3. doi: 10.1016/j.siny.2010.10.004. Epub 2010 Nov 3. Review.

PMID:
21051301

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