{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:11:21Z","timestamp":1787015481546,"version":"build-2736575974"},"reference-count":67,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2024,7,25]],"date-time":"2024-07-25T00:00:00Z","timestamp":1721865600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Midwife Womens Health"],"published-print":{"date-parts":[[2024,11]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Advances in technology have correlated with expanding prenatal genetic testing options for pregnant people. Leading medical organizations recommend cell\u2010free DNA as the most sensitive screening test for trisomies 13, 18, and 21, as well as for fetal sex chromosome aneuploidies. The commercially available testing options go beyond these recommended tests, and prenatal care professionals should be familiar with the tests that their patients may choose despite being beyond the scope of current medical recommendations. This article explains updates in cell\u2010free DNA technology and clinical considerations for prenatal care professionals, recognizing that this is a rapidly changing field of science and health care.<\/jats:p>","DOI":"10.1111\/jmwh.13674","type":"journal-article","created":{"date-parts":[[2024,7,25]],"date-time":"2024-07-25T23:29:42Z","timestamp":1721950182000},"page":"836-846","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Clinical Applications of Fetal Cell\u2010Free DNA: State of the Science"],"prefix":"10.1111","volume":"69","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7914-2295","authenticated-orcid":false,"given":"Julie","family":"Knutson","sequence":"first","affiliation":[{"name":"Division of Academic Midwifery Alpert Medical School of Brown University, Women &amp; Infants Hospital  Providence Rhode Island"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kathryn","family":"Anthony","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology Alpert Medical School of Brown University, Women &amp; Infants Hospital  Providence Rhode Island"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa L.","family":"Russo","sequence":"additional","affiliation":[{"name":"Division of Maternal Fetal Medicine Alpert Medical School of Brown University, Women &amp; Infants Hospital  Providence Rhode Island"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Martha B.","family":"Kole\u2010White","sequence":"additional","affiliation":[{"name":"Division of Maternal Fetal Medicine Alpert Medical School of Brown University, Women &amp; Infants Hospital  Providence Rhode Island"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2024,7,25]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1097\/AOG.0000000000004084"},{"key":"e_1_2_9_3_1","unstructured":"Prenatal genetic screening tests. 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