Literature DB >> 7837256

The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

A Clarke.   

Abstract

Entities:  

Keywords:  Clinical Genetics Society (Great Britain); Empirical Approach; Genetics and Reproduction

Mesh：

Year:  1994        PMID： 7837256      PMCID： PMC1050126          DOI： 10.1136/jmg.31.10.785

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  28 in total

1.  Stigmatization of carrier status: social implications of heterozygote genetic screening programs.

Authors:  R H Kenen; R M Schmidt
Journal:  Am J Public Health       Date:  1978-11       Impact factor: 9.308

2.  Uptake of presymptomatic predictive testing for Huntington's disease.

Authors:  D Craufurd; A Dodge; L Kerzin-Storrar; R Harris
Journal:  Lancet       Date:  1989-09-09       Impact factor: 79.321

3.  Problems in genetic prediction for Huntington's disease.

Authors:  M J Morris; A Tyler; L Lazarou; L Meredith; P S Harper
Journal:  Lancet       Date:  1989-09-09       Impact factor: 79.321

4.  Ethics of predictive testing for Huntington's chorea: the need for more information.

Authors:  D I Craufurd; R Harris
Journal:  Br Med J (Clin Res Ed)       Date:  1986-07-26

5.  Adoption and genetic prediction for Huntington's disease.

Authors:  M Morris; A Tyler; P S Harper
Journal:  Lancet       Date:  1988-11-05       Impact factor: 79.321

6.  Adoption, genetic disease, and DNA.

Authors:  P D Turnpenny; S A Simpson; A M McWhinnie
Journal:  Arch Dis Child       Date:  1993-10       Impact factor: 3.791

7.  A genetic register for Huntington's chorea in South Wales.

Authors:  P S Harper; A Tyler; S Smith; P Jones; R G Newcombe; V McBroom
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

8.  A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal.

Authors:  S Zeesman; C L Clow; L Cartier; C R Scriver
Journal:  Am J Med Genet       Date:  1984-08

9.  Psychological consequences of neonatal screening for alpha 1-antitrypsin deficiency. Parental reactions to the first news of their infants' deficiency.

Authors:  T Thelin; T F McNeil; E Aspegren-Jansson; T Sveger
Journal:  Acta Paediatr Scand       Date:  1985-09

10.  Invited essay on the psychological aspects of genetic counseling. V. Preselection: a family coping strategy in Huntington disease.

Authors:  S Kessler
Journal:  Am J Med Genet       Date:  1988-11
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  71 in total

Review 1.  Integrated regional genetic services: current and future provision.

Authors:  D Donnai; R Elles
Journal:  BMJ       Date:  2001-04-28

2.  GeneClinics: a hybrid text/data electronic publishing model using XML applied to clinical genetic testing.

Authors:  P Tarczy-Hornoch; P Shannon; P Baskin; M Espeseth; R A Pagon
Journal:  J Am Med Inform Assoc       Date:  2000 May-Jun       Impact factor: 4.497

3.  Counseling adolescents and the challenges for genetic counselors.

Authors:  Alice Callard; Jessica Williams; Heather Skirton
Journal:  J Genet Couns       Date:  2011-12-03       Impact factor: 2.537

Review 4.  Newborn screening: new developments, new dilemmas.

Authors:  N J Kerruish; S P Robertson
Journal:  J Med Ethics       Date:  2005-07       Impact factor: 2.903

Review 5.  Working up policy: the use of specific disease exemplars in formulating general principles governing childhood genetic testing.

Authors:  Paula Boddington; Susan Hogben
Journal:  Health Care Anal       Date:  2006-03

6.  Refusing to provide a prenatal test: can it ever be ethical? Time to re-think the autonomy of future individuals.

Authors:  Paul D Kelly
Journal:  BMJ       Date:  2006-12-02

7.  Refusing to provide a prenatal test: can it ever be ethical?

Authors:  Rony E Duncan; Bennett Foddy; Martin B Delatycki
Journal:  BMJ       Date:  2006-11-18

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

Authors:  Kelly E Ormond; Carol J Gill; Patrick Semik; Kristi L Kirschner
Journal:  J Genet Couns       Date:  2003-08       Impact factor: 2.537

9.  Fragile X screening: attitudes of genetic health professionals.

Authors:  Kruti Acharya; Lainie Friedman Ross
Journal:  Am J Med Genet A       Date:  2009-02-15       Impact factor: 2.802

10.  Genetic testing of children for familial cancers: a comparative legal perspective on consent, communication of information and confidentiality.

Authors:  Roy Gilbar
Journal:  Fam Cancer       Date:  2009-07-17       Impact factor: 2.375
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