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3. Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. Pereira S; Smith HS; Frankel LA; Christensen KD; Islam R; Robinson JO; Genetti CA; Blout Zawatsky CL; Zettler B; Parad RB; Waisbren SE; Beggs AH; Green RC; Holm IA; McGuire AL; JAMA Pediatr; 2021 Nov; 175(11):1132-1141. PubMed ID: 34424265 [TBL] [Abstract][Full Text] [Related]
4. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Ross LF; Clayton EW Pediatrics; 2019 Dec; 144(6):. PubMed ID: 31719124 [TBL] [Abstract][Full Text] [Related]
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13. Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol. Milko LV; Rini C; Lewis MA; Butterfield RM; Lin FC; Paquin RS; Powell BC; Roche MI; Souris KJ; Bailey DB; Berg JS; Powell CM Trials; 2018 Jun; 19(1):344. PubMed ID: 29950170 [TBL] [Abstract][Full Text] [Related]
14. Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant. Borghesi A; Mencarelli MA; Memo L; Ferrero GB; Bartuli A; Genuardi M; Stronati M; Villani A; Renieri A; Corsello G; Ital J Pediatr; 2017 Nov; 43(1):100. PubMed ID: 29100554 [TBL] [Abstract][Full Text] [Related]
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17. Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies. Johnston J; Lantos JD; Goldenberg A; Chen F; Parens E; Koenig BA; Hastings Cent Rep; 2018 Jul; 48 Suppl 2(Suppl 2):S2-S6. PubMed ID: 30133723 [TBL] [Abstract][Full Text] [Related]
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19. Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project. Downie L; Halliday J; Lewis S; Lunke S; Lynch E; Martyn M; Gaff C; Jarmolowicz A; Amor DJ Genet Med; 2020 May; 22(5):937-944. PubMed ID: 31974413 [TBL] [Abstract][Full Text] [Related]
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