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2. Parents of a child with epilepsy: Views and expectations on receiving genetic results from Whole Genome Sequencing. Jaitovich Groisman I; Hurlimann T; Godard B Epilepsy Behav; 2019 Jan; 90():178-190. PubMed ID: 30583270 [TBL] [Abstract][Full Text] [Related]
3. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. Jamal L; Robinson JO; Christensen KD; Blumenthal-Barby J; Slashinski MJ; Perry DL; Vassy JL; Wycliff J; Green RC; McGuire AL AJOB Empir Bioeth; 2017; 8(2):82-88. PubMed ID: 28949844 [TBL] [Abstract][Full Text] [Related]
4. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders. Rosell AM; Pena LD; Schoch K; Spillmann R; Sullivan J; Hooper SR; Jiang YH; Mathey-Andrews N; Goldstein DB; Shashi V J Genet Couns; 2016 Oct; 25(5):1019-31. PubMed ID: 26868367 [TBL] [Abstract][Full Text] [Related]
5. Parents perspectives on whole genome sequencing for their children: qualified enthusiasm? Anderson JA; Meyn MS; Shuman C; Zlotnik Shaul R; Mantella LE; Szego MJ; Bowdin S; Monfared N; Hayeems RZ J Med Ethics; 2017 Aug; 43(8):535-539. PubMed ID: 27888232 [TBL] [Abstract][Full Text] [Related]
6. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis. Pucel J; Briere LC; Reuter C; Gochyyev P; ; LeBlanc K Genet Med; 2024 Jun; 26(6):101115. PubMed ID: 38436216 [TBL] [Abstract][Full Text] [Related]
8. Public attitudes in Japan toward participation in whole genome sequencing studies. Okita T; Ohashi N; Kabata D; Shintani A; Kato K Hum Genomics; 2018 Apr; 12(1):21. PubMed ID: 29653595 [TBL] [Abstract][Full Text] [Related]
9. [Whole exome sequencing and whole genome sequencing in undiagnosed disease: of value for certain patient populations]. Linthorst GE; Hollak CEM Ned Tijdschr Geneeskd; 2019 May; 163():. PubMed ID: 31120221 [TBL] [Abstract][Full Text] [Related]
10. Exome sequencing a review of new strategies for rare genomic disease research. Brown TL; Meloche TM Genomics; 2016 Oct; 108(3-4):109-114. PubMed ID: 27387609 [TBL] [Abstract][Full Text] [Related]
11. "We don't know her history, her background": adoptive parents' perspectives on whole genome sequencing results. Crouch J; Yu JH; Shankar AG; Tabor HK J Genet Couns; 2015 Feb; 24(1):67-77. PubMed ID: 25011977 [TBL] [Abstract][Full Text] [Related]
12. Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls. McInerney-Leo AM; Duncan EL Front Endocrinol (Lausanne); 2020; 11():628946. PubMed ID: 33679611 [TBL] [Abstract][Full Text] [Related]
14. Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis. Basel D; McCarrier J Pediatr Clin North Am; 2017 Feb; 64(1):265-272. PubMed ID: 27894449 [TBL] [Abstract][Full Text] [Related]
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