172 related articles for article (PubMed ID: 30133727)
21. Examination of the communication practices between state newborn screening programs and the medical home.
Kim S; Lloyd-Puryear MA; Tonniges TF
Pediatrics; 2003 Feb; 111(2):E120-6. PubMed ID: 12563084
[TBL] [Abstract][Full Text] [Related]
22. Genetic profiling of newborns: ethical and social issues.
Almond B
Nat Rev Genet; 2006 Jan; 7(1):67-71. PubMed ID: 16369573
[TBL] [Abstract][Full Text] [Related]
23. Lessons for Sequencing from the Addition of Severe Combined Immunodeficiency to Newborn Screening Panels.
Puck JM
Hastings Cent Rep; 2018 Jul; 48 Suppl 2(Suppl 2):S7-S9. PubMed ID: 30133735
[TBL] [Abstract][Full Text] [Related]
24. Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project.
Genetti CA; Schwartz TS; Robinson JO; VanNoy GE; Petersen D; Pereira S; Fayer S; Peoples HA; Agrawal PB; Betting WN; Holm IA; McGuire AL; Waisbren SE; Yu TW; Green RC; Beggs AH; Parad RB;
Genet Med; 2019 Mar; 21(3):622-630. PubMed ID: 30209271
[TBL] [Abstract][Full Text] [Related]
25. Doctors explore research potential of blood samples from newborns.
Roehr B
BMJ; 2009 Sep; 339():b3984. PubMed ID: 19786491
[No Abstract] [Full Text] [Related]
26. Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.
Berg JS; Powell CM
Cold Spring Harb Perspect Med; 2015 Oct; 5(12):. PubMed ID: 26438605
[TBL] [Abstract][Full Text] [Related]
27. [Ethical aspects of neonatal genetic screening].
Feito Grande L
Rev Derecho Genoma Hum; 2010; (32):221-41. PubMed ID: 21192438
[TBL] [Abstract][Full Text] [Related]
28. The Reproductive Journey in the Genomic Era: From Preconception to Childhood.
Garcia-Herrero S; Simon B; Garcia-Planells J
Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33352697
[TBL] [Abstract][Full Text] [Related]
29. Provision of information about newborn screening antenatally: a sequential exploratory mixed-methods project.
Ulph F; Wright S; Dharni N; Payne K; Bennett R; Roberts S; Walshe K; Lavender T
Health Technol Assess; 2017 Oct; 21(55):1-240. PubMed ID: 28967862
[TBL] [Abstract][Full Text] [Related]
30. A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.
Cakici JA; Dimmock DP; Caylor SA; Gaughran M; Clarke C; Triplett C; Clark MM; Kingsmore SF; Bloss CS
Am J Hum Genet; 2020 Nov; 107(5):953-962. PubMed ID: 33157008
[TBL] [Abstract][Full Text] [Related]
31. The future of Cochrane Neonatal.
Soll RF; Ovelman C; McGuire W
Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
[TBL] [Abstract][Full Text] [Related]
32. Neonatal genetic testing is more than screening.
Kenner C; Lewis JA; Pressler JL; Little CM
Crit Care Nurs Clin North Am; 2008 Jun; 20(2):233-7, vii. PubMed ID: 18424352
[TBL] [Abstract][Full Text] [Related]
33. Single-Gene Sequencing in Newborn Screening: Success, Challenge, Hope.
Currier RJ
Hastings Cent Rep; 2018 Jul; 48 Suppl 2(Suppl 2):S37-S38. PubMed ID: 30133731
[TBL] [Abstract][Full Text] [Related]
34. Parents' interest in whole-genome sequencing of newborns.
Goldenberg AJ; Dodson DS; Davis MM; Tarini BA
Genet Med; 2014 Jan; 16(1):78-84. PubMed ID: 23743552
[TBL] [Abstract][Full Text] [Related]
35. Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges.
Hill M; Hammond J; Lewis C; Mellis R; Clement E; Chitty LS
Eur J Hum Genet; 2020 Nov; 28(11):1529-1540. PubMed ID: 32561901
[TBL] [Abstract][Full Text] [Related]
36. Technology and the environment: supportive resource or barrier for people with developmental disabilities?
Hammel J
Nurs Clin North Am; 2003 Jun; 38(2):331-49. PubMed ID: 12914311
[TBL] [Abstract][Full Text] [Related]
37. Managing sickle cell carrier results generated through newborn screening in Ontario: a precedent-setting policy story.
Hayeems RZ; Moore Hepburn C; Chakraborty P; Odame I; Clarke J; Miller FA; Brown AD
Genet Med; 2017 Jun; 19(6):625-627. PubMed ID: 27763632
[No Abstract] [Full Text] [Related]
38. Discouraging Elective Genetic Testing of Minors: A Norm under Siege in a New Era of Genomic Medicine.
Hercher L
Cold Spring Harb Perspect Med; 2020 May; 10(5):. PubMed ID: 31548217
[TBL] [Abstract][Full Text] [Related]
39. [Genomic newborn screening. Perspective from the Ethics commission of the Spanish Society for Human Genetics. Part I. Next generation sequencing technologies applied to newborn screening. Challenges and opportunities.].
Pàmpols Ros T; Pérez Aytés A; García Sagredo JM; Díaz de Bustamante A; Blanco Guillermo I
Rev Esp Salud Publica; 2022 Feb; 96():. PubMed ID: 35115483
[TBL] [Abstract][Full Text] [Related]
40. Challenges of using next generation sequencing in newborn screening.
Reinstein E
Genet Res (Camb); 2015 Nov; 97():e21. PubMed ID: 26521961
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
