Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 17

1.

Genetics and cardiovascular disease: a policy statement from the American Heart Association.

Ashley EA, Hershberger RE, Caleshu C, Ellinor PT, Garcia JG, Herrington DM, Ho CY, Johnson JA, Kittner SJ, Macrae CA, Mudd-Martin G, Rader DJ, Roden DM, Scholes D, Sellke FW, Towbin JA, Van Eyk J, Worrall BB; American Heart Association Advocacy Coordinating Committee.

Circulation. 2012 Jul 3;126(1):142-57. doi: 10.1161/CIR.0b013e31825b07f8. Epub 2012 May 29. No abstract available.

2.

Ethical issues of predictive genetic testing for diabetes.

Haga SB.

J Diabetes Sci Technol. 2009 Jul 1;3(4):781-8. Review.

3.

Civilian and military genetics: nondiscrimination policy in a post-GINA world.

Baruch S, Hudson K.

Am J Hum Genet. 2008 Oct;83(4):435-44. doi: 10.1016/j.ajhg.2008.09.003.

4.

Fear of health insurance loss among individuals at risk for Huntington disease.

Oster E, Dorsey ER, Bausch J, Shinaman A, Kayson E, Oakes D, Shoulson I, Quaid K; Huntington Study Group PHAROS Investigators.

Am J Med Genet A. 2008 Aug 15;146A(16):2070-7. doi: 10.1002/ajmg.a.32422.

5.

Access to health insurance: experiences and attitudes of those with genetic versus non-genetic medical conditions.

Kass NE, Medley AM, Natowicz MR, Hull SC, Faden RR, Plantinga L, Gostin LO.

Am J Med Genet A. 2007 Apr 1;143A(7):707-17.

6.

Racial differences in beliefs about genetic screening among patients at inner-city neighborhood health centers.

Zimmerman RK, Tabbarah M, Nowalk MP, Raymund M, Jewell IK, Wilson SA, Ricci EM.

J Natl Med Assoc. 2006 Mar;98(3):370-7.

7.

Development and validation of tools to assess genetic discrimination and genetically based racism.

Parrott RL, Silk KJ, Dillow MR, Krieger JL, Harris TM, Condit CM.

J Natl Med Assoc. 2005 Jul;97(7):980-90.

8.

Direct-to-consumer sales of genetic services on the Internet.

Gollust SE, Wilfond BS, Hull SC.

Genet Med. 2003 Jul-Aug;5(4):332-7.

9.

Why should primary care physicians know about the genetics of dementia?

Pinsky LE, Burke W, Bird TD.

West J Med. 2001 Dec;175(6):412-6. Review. No abstract available.

10.
11.

The role of community review in evaluating the risks of human genetic variation research.

Foster MW, Sharp RR, Freeman WL, Chino M, Bernsten D, Carter TH.

Am J Hum Genet. 1999 Jun;64(6):1719-27.

12.

Should we genetically test everyone for haemochromatosis?

Allen K, Williamson R.

J Med Ethics. 1999 Apr;25(2):209-14.

13.
14.

Genetics and the British insurance industry.

Cook ED.

J Med Ethics. 1999 Apr;25(2):157-62.

15.

Genetic testing and public policy.

Holtzman NA, Shapiro D.

BMJ. 1998 Mar 14;316(7134):852-6. Review. No abstract available.

16.

Questioning the need for anonymous genetic counseling and testing.

Uhlmann WR, Ginsburg D, Gelehrter TD, Nicholson J, Petty EM.

Am J Hum Genet. 1996 Oct;59(4):968-70. No abstract available.

17.

Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.

FitzGerald MG, Harkin DP, Silva-Arrieta S, MacDonald DJ, Lucchina LC, Unsal H, O'Neill E, Koh J, Finkelstein DM, Isselbacher KJ, Sober AJ, Haber DA.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8541-5.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk