These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 32163096)
41. Genetic counseling for families of patients with fragile X syndrome. Barrett SK; Drazin T; Rosa D; Kupchik GS JAMA; 2004 Jun; 291(24):2945; author reply 2945-6. PubMed ID: 15213204 [No Abstract] [Full Text] [Related]
42. Ethics, genetics and science policy. Tranoy KE Bull Med Ethics; 1992 Apr; (77):13-20. PubMed ID: 15997530 [TBL] [Abstract][Full Text] [Related]
43. Issues in genetic testing of children. Twomey JG MCN Am J Matern Child Nurs; 2006; 31(3):156-63. PubMed ID: 16679956 [TBL] [Abstract][Full Text] [Related]
44. Genetic testing for hereditary cancer: challenges to ethical care in rural and remote communities. D'Agincourt-Canning L HEC Forum; 2004 Dec; 16(4):222-33. PubMed ID: 15672697 [No Abstract] [Full Text] [Related]
46. Ethical aspects of early diagnosis of genetic diseases. Berg K World Health; 1996; 49(5):20-1. PubMed ID: 17333578 [No Abstract] [Full Text] [Related]
47. Genomic testing: a struggle for oncologists. Hede K J Natl Cancer Inst; 2014 Jun; 106(6):dju172. PubMed ID: 24907388 [No Abstract] [Full Text] [Related]
48. Advancing Global Precision Medicine: An Overview of Genomic Testing and Counseling Services in Malaysia. Balasopoulou A; Mooy FM; Baker DJ; Mitropoulou C; Skoufas E; Bulgiba A; Katsila T; Patrinos GP OMICS; 2017 Dec; 21(12):733-740. PubMed ID: 29173101 [TBL] [Abstract][Full Text] [Related]
49. [Confidentiality, genetic counseling, and public health: a case study on sickle cell trait]. Diniz D; Guedes C Cad Saude Publica; 2005; 21(3):747-55. PubMed ID: 15868032 [TBL] [Abstract][Full Text] [Related]
50. Moral issues arising from genetics. Zucker A; Patriquin D Listening; 1987; 22(1):65-85. PubMed ID: 16127843 [TBL] [Abstract][Full Text] [Related]
51. Prenatal genetic testing and wrongful birth lawsuits. DuBois JM Health Care Ethics USA; 2001; 9(2):E1. PubMed ID: 16184687 [No Abstract] [Full Text] [Related]
52. Genetic testing in neuromuscular disease. Krajewski KM; Shy ME Neurol Clin; 2004 Aug; 22(3):481-508, v. PubMed ID: 15207873 [TBL] [Abstract][Full Text] [Related]
53. [Individualized, personalized and stratified medicine: a challenge for allergology in ENT?]. Chaker AM; Klimek L HNO; 2015 May; 63(5):334-42. PubMed ID: 25940007 [TBL] [Abstract][Full Text] [Related]
55. Population Whole Exome Screening: Primary Care Provider Attitudes About Preparedness, Information Avoidance, and Nudging. Heck PR; Meyer MN Med Clin North Am; 2019 Nov; 103(6):1077-1092. PubMed ID: 31582005 [TBL] [Abstract][Full Text] [Related]
56. [Bioethics in gene diagnosis and gene therapy]. Takebe H Nihon Rinsho; 2005 Dec; 63 Suppl 12():477-80. PubMed ID: 16416838 [No Abstract] [Full Text] [Related]
58. Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Schmidlen T; Sturm AC; Hovick S; Scheinfeldt L; Scott Roberts J; Morr L; McElroy J; Toland AE; Christman M; O'Daniel JM; Gordon ES; Bernhardt BA; Ormond KE; Sweet K J Genet Couns; 2018 Sep; 27(5):1111-1129. PubMed ID: 29460110 [TBL] [Abstract][Full Text] [Related]
59. Ethical Implications of Direct-to-Consumer Hereditary Cancer Tests. Kilbride MK; Domchek SM; Bradbury AR JAMA Oncol; 2018 Oct; 4(10):1327-1328. PubMed ID: 30027223 [No Abstract] [Full Text] [Related]
60. Ethical considerations of population screening for late-onset genetic disease. Golden-Grant K; Merritt JL; Scott CR Clin Genet; 2015 Dec; 88(6):589-92. PubMed ID: 25677830 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]