{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T18:58:10Z","timestamp":1790794690281,"version":"4.1.0"},"reference-count":28,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2003,4,11]],"date-time":"2003-04-11T00:00:00Z","timestamp":1050019200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2003,7,15]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The ability to perform predictive genetic testing of children raises ethical concerns. Current guidelines support the screening of newborns for conditions in which early treatment reduces morbidity and mortality, and oppose most other predictive genetic screening and testing in childhood. Little is known, however, about parental attitudes. We conducted focus groups to gain information on the attitudes, beliefs, and concerns of parents about newborn screening and testing for both treatable and untreatable conditions that present in childhood. Respondents across racial groups support mandatory newborn screening for treatable conditions like phenylketonuria (PKU), citing lack of parental knowledge, and concerns about immature parental decision\u2010makers. Parents do, however, want more information. Citing a variety of psychosocial concerns, respondents believe that parents should have access to predictive genetic testing for childhood onset conditions, even when there are no proven treatments. Respondents want this information to make reproductive and non\u2010reproductive plans and decisions. Although respondents varied in their personal interest in testing, overwhelmingly they believed that the decisions belong to the parents. Professional guidelines that proscribe predictive testing for untreatable childhood onset conditions should be re\u2010examined in light of consumer attitudes. \u00a9 2003 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.20031","type":"journal-article","created":{"date-parts":[[2003,6,24]],"date-time":"2003-06-24T10:15:25Z","timestamp":1056449725000},"page":"209-214","source":"Crossref","is-referenced-by-count":62,"title":["Parental attitudes regarding newborn screening of PKU and DMD"],"prefix":"10.1002","volume":"120A","author":[{"given":"Elizabeth","family":"Campbell","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lainie Friedman","family":"Ross","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2003,4,11]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.107.6.1451"},{"key":"e_1_2_6_3_1","first-page":"1233","article-title":"Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents","volume":"57","author":"American Society of Human Genetics (ASHG)\/American College of Medical Genetics (ACMG)","year":"1995","journal-title":"Am J Hum Genet"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.2307\/3562038"},{"key":"e_1_2_6_5_1","first-page":"519","article-title":"Practice guidelines for clinical prevention: Do patients, physicians, and experts share common ground?","volume":"161","author":"Beaulieu MD","year":"1999","journal-title":"CMAJ"},{"key":"e_1_2_6_6_1","first-page":"476","article-title":"Discrimination as a consequence of genetic testing","volume":"50","author":"Billings PR","year":"1992","journal-title":"Am J Hum Genet"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(98)05279-9"},{"key":"e_1_2_6_8_1","unstructured":"CampbellE RossLF.2003.Parental attitudes and beliefs regarding the genetic testing of children. 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