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1.
A logic model for precision medicine implementation informed by stakeholder views and implementation science.
Genet Med
; 21(5): 1139-1154, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30353149
2.
Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions.
Genet Med
; 21(6): 1371-1380, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30377384
3.
Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists.
Genet Med
; 19(1): 112-120, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27362912
4.
Reporting genomic secondary findings: ACMG members weigh in.
Genet Med
; 17(1): 27-35, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25394173
5.
A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians.
Genet Med
; 16(1): 60-9, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23765051
6.
Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndrome.
Am J Med Genet A
; 164A(12): 3076-82, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25256560
7.
Cleft Lip and Palate in a Patient with 5q35.2-q35.3 Microdeletion: The Importance of Chromosomal Microarray Testing in the Craniofacial Clinic.
Cleft Palate Craniofac J
; 50(5): 618-22, 2013 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22449124
8.
An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency.
Mol Genet Metab
; 101(4): 413-6, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20817516
9.
Integrating Germline Genetics Into Precision Oncology Practice in the Veterans Health Administration: Challenges and Opportunities.
Fed Pract
; 37(Suppl 4): S82-S88, 2020 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-32908356
10.
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.
Case Rep Genet
; 2011: 131768, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-23074670
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