{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,28]],"date-time":"2023-09-28T09:44:38Z","timestamp":1695894278177},"reference-count":26,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2010,12,24]],"date-time":"2010-12-24T00:00:00Z","timestamp":1293148800000},"content-version":"vor","delay-in-days":2058,"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":[[2005,5,6]]},"abstract":"<jats:p>The integration of universal cystic fibrosis screening in women's health has considerably altered the way we care for obstetric patients and likely will be the foundation for incorporating other genetic tests into routine women's health care. Prior to this change in the standard of care, screening for genetic disease was primarily limited to those individuals who had a personal or family history of the genetic condition or who belonged to a particular ethnic or racial group characterized by a high frequency of carrier and affected individuals. However, technological advances have resulted in facile and economic methodologies for detecting an increasing number of genetic mutations and in the realization that screening for common and uncommon disorders will likely be a not\u2010too\u2010distant\u2010future part of routine health care. Programs that permit clinicians to properly implement genetic protocols and allow patients to make informed decisions about genetic screening and diagnostic tests are needed. The implementation of universal cystic fibrosis screening allows clinicians to recognize the benefits and pitfalls of genetic testing of the general population and encourages the development of programs that will effectively communicate genetic information to professionals and laity.<\/jats:p>","DOI":"10.1016\/j.jmwh.2004.12.015","type":"journal-article","created":{"date-parts":[[2005,7,19]],"date-time":"2005-07-19T14:39:28Z","timestamp":1121783968000},"page":"205-210","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Cystic Fibrosis Screening"],"prefix":"10.1111","volume":"50","author":[{"given":"Lee P.","family":"Shulman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2010,12,24]]},"reference":[{"key":"e_1_2_9_2_2","volume-title":"American College of Medical Genetics","author":"American College of Obstetricians and Gynecologists","year":"2001"},{"key":"e_1_2_9_3_2","doi-asserted-by":"publisher","DOI":"10.1258\/096914103769010978"},{"key":"e_1_2_9_4_2","doi-asserted-by":"publisher","DOI":"10.1001\/archinte.159.14.1529"},{"key":"e_1_2_9_5_2","doi-asserted-by":"publisher","DOI":"10.1067\/mpd.2002.127666"},{"key":"e_1_2_9_6_2","first-page":"RR\u201016","article-title":"Newborn screening for cystic fibrosis: A paradigm for public health policy development","volume":"46","author":"Centers for Disease Control and Prevention.","year":"1997","journal-title":"MMWR"},{"key":"e_1_2_9_7_2","doi-asserted-by":"publisher","DOI":"10.1097\/01.GIM.0000139509.04177.4B"},{"key":"e_1_2_9_8_2","doi-asserted-by":"publisher","DOI":"10.1002\/pd.618"},{"key":"e_1_2_9_9_2","doi-asserted-by":"publisher","DOI":"10.1093\/aje\/kwh083"},{"key":"e_1_2_9_10_2","volume-title":"Patient registry annual report 1994","author":"Cystic Fibrosis Foundation.","year":"2000"},{"key":"e_1_2_9_11_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0095-5108(05)70090-7"},{"key":"e_1_2_9_12_2","first-page":"443","article-title":"Genetic analysis of Hispanic individuals with cystic fibrosis","volume":"54","author":"Grebe TA","year":"1994","journal-title":"Am J Hum Genet"},{"key":"e_1_2_9_13_2","first-page":"433","article-title":"Cystic fibrosis mutations among African\u2010Americans in the southeastern United States","volume":"87","author":"Phillips OP","year":"1995","journal-title":"J Natl Med Assoc"},{"key":"e_1_2_9_14_2","first-page":"525","article-title":"Genotypes of cystic fibrosis (CF) in the world and polymorphisms of cystic fibrosis transmembrane regulator (CFTR) gene in Japan","volume":"54","author":"Wang W","year":"1996","journal-title":"Nippon Rinsho"},{"key":"e_1_2_9_15_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.2475911"},{"key":"e_1_2_9_16_2","doi-asserted-by":"publisher","DOI":"10.1016\/0888-7543(91)90503-7"},{"key":"e_1_2_9_17_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.2570460"},{"key":"e_1_2_9_18_2","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1098-1004(1997)10:2<135::AID-HUMU6>3.0.CO;2-J"},{"key":"e_1_2_9_19_2","first-page":"1122","article-title":"Identification of common cystic fibrosis mutations in African\u2010Americans with cystic fibrosis increases the detection rate to 75%","volume":"9","author":"Macek M","year":"1997","journal-title":"Am J Hum Genet"},{"key":"e_1_2_9_20_2","first-page":"951","article-title":"Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population","volume":"51","author":"Abeliovich D","year":"1992","journal-title":"Am J Hum Genet"},{"key":"e_1_2_9_21_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0025-7125(05)70243-1"},{"key":"e_1_2_9_22_2","doi-asserted-by":"publisher","DOI":"10.1002\/humu.1380040409"},{"key":"e_1_2_9_23_2","doi-asserted-by":"publisher","DOI":"10.1016\/0168-9525(92)90168-4"},{"key":"e_1_2_9_24_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10431"},{"key":"e_1_2_9_25_2","doi-asserted-by":"publisher","DOI":"10.1089\/109065701753145574"},{"key":"e_1_2_9_26_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.20259"},{"key":"e_1_2_9_27_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199406023302213"}],"container-title":["Journal of Midwifery &amp; 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