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    Results: 19

    1.

    Diversity in genetic counseling: past, present and future.

    Warren NS, Ormond KE.

    J Genet Couns. 2009 Apr;18(2):197-9. Epub 2009 Feb 25. No abstract available. PMID: 19241151 [PubMed - indexed for MEDLINE]Related articles

    2.

    Assessing the understanding of biobank participants.

    Ormond KE, Cirino AL, Helenowski IB, Chisholm RL, Wolf WA.

    Am J Med Genet A. 2009 Feb;149A(2):188-98.PMID: 19161150 [PubMed - indexed for MEDLINE]Related articles

    3.

    Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening.

    Ormond KE, Banuvar S, Daly A, Iris M, Minogue J, Elias S.

    Patient Educ Couns. 2009 May;75(2):244-50. Epub 2008 Nov 14.PMID: 19013744 [PubMed - indexed for MEDLINE]Related articles

    4.

    Medical ethics for the genome world: a paper from the 2007 William Beaumont hospital symposium on molecular pathology.

    Ormond KE.

    J Mol Diagn. 2008 Sep;10(5):377-82. Epub 2008 Aug 7. Review.PMID: 18687790 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Association of spinocerebellar ataxia type 3 and spinocerebellar ataxia type 8 microsatellite expansions: genetic counseling implications.

    Paganoni S, Seelaus CA, Ormond KE, Opal P.

    Mov Disord. 2008 Jan;23(1):154-5. No abstract available. PMID: 17987652 [PubMed - indexed for MEDLINE]Related articles

    6.

    The next exclusion debate: assessing technology, ethics, and intellectual disability after the Human Genome Project.

    Munger KM, Gill CJ, Ormond KE, Kirschner KL.

    Ment Retard Dev Disabil Res Rev. 2007;13(2):121-8. Review.PMID: 17563891 [PubMed - indexed for MEDLINE]Related articles

    7.

    What do patients prefer: informed consent models for genetic carrier testing.

    Ormond KE, Iris M, Banuvar S, Minogue J, Annas GJ, Elias S.

    J Genet Couns. 2007 Aug;16(4):539-50. Epub 2007 May 11.PMID: 17492496 [PubMed - indexed for MEDLINE]Related articles

    8.

    Outcome of chromosomally abnormal pregnancies in Lebanon: obstetricians' roles during and after prenatal diagnosis.

    Eldahdah LT, Ormond KE, Nassar AH, Khalil T, Zahed LF.

    Prenat Diagn. 2007 Jun;27(6):525-34.PMID: 17367106 [PubMed - indexed for MEDLINE]Related articles

    9.

    Disclosing genetic research results: examples from practice.

    Ormond KE.

    Am J Bioeth. 2006 Nov-Dec;6(6):30-2; author reply W10-2. No abstract available. PMID: 17085402 [PubMed - indexed for MEDLINE]Related articles

    10.

    Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.

    Hiraki S, Ormond KE, Kim K, Ross LF.

    Am J Med Genet A. 2006 Nov 1;140(21):2312-9.PMID: 17036312 [PubMed - indexed for MEDLINE]Related articles

    11.

    Genetic risk assessment and BRCA mutation testing.

    Ormond KE, Bellcross C, Weissman S.

    Ann Intern Med. 2006 Feb 21;144(4):303-4; discussion 304. No abstract available. PMID: 16490919 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing program.

    Hegwer G, Fairley C, Charrow J, Ormond KE.

    J Genet Couns. 2006 Feb;15(1):61-70.PMID: 16468087 [PubMed - indexed for MEDLINE]Related articles

    13.

    Marshall-Smith syndrome: natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities.

    Adam MP, Hennekam RC, Keppen LD, Bull MJ, Clericuzio CL, Burke LW, Ormond KE, Hoyme EH.

    Am J Med Genet A. 2005 Aug 30;137(2):117-24. Review.PMID: 16086394 [PubMed - indexed for MEDLINE]Related articles

    14.

    Outline of a medical genetics curriculum for internal medicine residency training programs.

    Riegert-Johnson DL, Korf BR, Alford RL, Broder MI, Keats BJ, Ormond KE, Pyeritz RE, Watson MS.

    Genet Med. 2004 Nov-Dec;6(6):543-7.PMID: 15545754 [PubMed - indexed for MEDLINE]Related articles

    15.

    Adjunct prenatal testing: patient decisions regarding ethnic carrier screening and fluorescence in situ hybridization.

    Sturm EL, Ormond KE.

    J Genet Couns. 2004 Feb;13(1):45-63.PMID: 19731471 [PubMed - indexed for MEDLINE]Related articles

    16.

    Attitudes of health care trainees about genetics and disability: issues of access, health care communication, and decision making.

    Ormond KE, Gill CJ, Semik P, Kirschner KL.

    J Genet Couns. 2003 Aug;12(4):333-49.PMID: 14682357 [PubMed - indexed for MEDLINE]Related articles

    17.

    Effect of family history on disclosure patterns of cystic fibrosis carrier status.

    Ormond KE, Mills PL, Lester LA, Ross LF.

    Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):70-7.PMID: 12704640 [PubMed - indexed for MEDLINE]Related articles

    18.

    The genetic family history as a risk assessment tool in internal medicine.

    Frezzo TM, Rubinstein WS, Dunham D, Ormond KE.

    Genet Med. 2003 Mar-Apr;5(2):84-91.PMID: 12644777 [PubMed - indexed for MEDLINE]Related articles

    19.

    The impact of genetic technologies on perceptions of disability.

    Kirschner KL, Ormond KE, Gill CJ.

    Qual Manag Health Care. 2000 Spring;8(3):19-26. Review.PMID: 10947381 [PubMed - indexed for MEDLINE]Related articles

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