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Items: 8


A framework for assessing outcomes from newborn screening: on the road to measuring its promise.

Hinton CF, Homer CJ, Thompson AA, Williams A, Hassell KL, Feuchtbaum L, Berry SA, Comeau AM, Therrell BL, Brower A, Harris KB, Brown C, Monaco J, Ostrander RJ, Zuckerman AE, Kaye C, Dougherty D, Greene C, Green NS; Follow-up and Treatment Sub-committee of the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC).

Mol Genet Metab. 2016 Aug;118(4):221-9. doi: 10.1016/j.ymgme.2016.05.017. Epub 2016 May 31.


Understanding Genetics: A New York, Mid-Atlantic Guide for Patients and Health Professionals.

Genetic Alliance, The New York-Mid-Atlantic Consortium for Genetic and Newborn Screening Services.

Washington (DC): Genetic Alliance; 2009 Jul 8.


Making Sense of Your Genes: A Guide to Genetic Counselling.

National Society of Genetic Counselors, Genetic Alliance.

Washington (DC): Genetic Alliance; 2008.


Why physicians should know the legal and ethical issues raised by genetic information and technology.

Lagay F.

Virtual Mentor. 2000 Nov 1;2(11). pii: virtualmentor.2000.2.11.gnth1-0011. doi: 10.1001/virtualmentor.2000.2.11.gnth1-0011. No abstract available.


Advisory committee on heritable disorders and genetic diseases in newborns and children.

Howell RR; Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children.

Ment Retard Dev Disabil Res Rev. 2006;12(4):313-5. No abstract available.


DNA-sequence patenting: National Society of Genetic Counselors (NSGC) position paper.

McIntosh N, Braddock BR, Branda KJ, Eanet K, Goldberg S, Kieffer SA, Primiano L, Quercia N, Taylor KA, Tsipis J, Yashar BM, Yesley A; National Society of Genetic Counselors DNA Sequence Patenting Position Paper Working Group.

J Genet Couns. 2002 Aug;11(4):241-3.


Disclosure of familial genetic information: perceptions of the duty to inform.

Lehmann LS, Weeks JC, Klar N, Biener L, Garber JE.

Am J Med. 2000 Dec 15;109(9):705-11.


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