Detalhe da pesquisa
1.
The impact of false-positive newborn screening results on families: a qualitative study.
Genet Med
; 14(1): 76-80, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22237434
2.
A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: recommendations of the United States secretary for health and human services advisory committee on heritable disorders in newborns and children.
Genet Med
; 12(2): 77-80, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20084011
3.
Long-term outcomes of the "Genetics in Primary Care" faculty development initiative.
Fam Med
; 41(4): 266-70, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19343557
4.
Educational needs in genetic medicine: primary care perspectives.
Community Genet
; 11(3): 160-5, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18376112
5.
Healthy choices through family history: a community approach to family history awareness.
Community Genet
; 11(6): 343-51, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18690002
6.
Personalizing prenatal care using family health history: identifying a panel of conditions for a novel electronic genetic screening tool.
Per Med
; 10(3): 307-318, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29768747
7.
Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts.
Pediatrics
; 117(5 Pt 2): S326-40, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16735260
8.
Attitudes about genetics in underserved, culturally diverse populations.
Community Genet
; 8(3): 161-72, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16113533