Μη επεμβατικός προγεννητικός έλεγχος (Greek Wikipedia)

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«Redirecting». linkinghub.elsevier.com. Ανακτήθηκε στις 27 Ιουνίου 2021.

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Rose, Nancy C.; Kaimal, Anjali J.; Dugoff, Lorraine; Norton, Mary E.; Medicin, American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins-ObstetricsCommittee on GeneticsSociety for Maternal-Fetal (2020-10). «Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin, Number 226» (στα αγγλικά). Obstetrics & Gynecology 136 (4): e48. doi:10.1097/AOG.0000000000004084. ISSN 0029-7844. https://journals.lww.com/greenjournal/Fulltext/2020/10000/Screening_for_Fetal_Chromosomal_Abnormalities_.44.aspx.

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Palomaki, Glenn E.; Deciu, Cosmin; Kloza, Edward M.; Lambert-Messerlian, Geralyn M.; Haddow, James E.; Neveux, Louis M.; Ehrich, Mathias; van den Boom, Dirk και άλλοι. (2012-03). «DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study» (στα αγγλικά). Genetics in Medicine 14 (3): 296–305. doi:10.1038/gim.2011.73. ISSN 1530-0366. https://www.nature.com/articles/gim201173.

nih.gov

Dondorp, Wybo; de Wert, Guido; Bombard, Yvonne; Bianchi, Diana W; Bergmann, Carsten; Borry, Pascal; Chitty, Lyn S; Fellmann, Florence και άλλοι. (2015-10). «Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening». European Journal of Human Genetics 23 (11): 1438–1450. doi:10.1038/ejhg.2015.57. ISSN 1018-4813. PMID 25782669. PMC 4613463. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613463/.
Allyse, Megan; Minear, Mollie A; Berson, Elisa; Sridhar, Shilpa; Rote, Margaret; Hung, Anthony; Chandrasekharan, Subhashini (2015-01-16). «Non-invasive prenatal testing: a review of international implementation and challenges». International Journal of Women's Health 7: 113–126. doi:10.2147/IJWH.S67124. ISSN 1179-1411. PMID 25653560. PMC 4303457. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303457/.
Zimmermann, Bernhard; Hill, Matthew; Gemelos, George; Demko, Zachary; Banjevic, Milena; Baner, Johan; Ryan, Allison; Sigurjonsson, Styrmir και άλλοι. (2012-12). «Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci». Prenatal Diagnosis 32 (13): 1233–1241. doi:10.1002/pd.3993. ISSN 1097-0223. PMID 23108718. PMC 3548605. https://pubmed.ncbi.nlm.nih.gov/23108718/.

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Μη επεμβατικός προγεννητικός έλεγχος (Greek Wikipedia)

doi.org

dx.doi.org

doi.org

elsevier.com

linkinghub.elsevier.com

fertstert.org

lww.com

journals.lww.com

medlineplus.gov

nature.com

nih.gov

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

pubmedcentral.nih.gov

sciencedirect.com

web.archive.org

wiley.com

obgyn.onlinelibrary.wiley.com

worldcat.org