Literature DB >> 7646731

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants. A positive screening test for an untreatable condition provides psychological relief from uncertainty.

T Marteau, S Michie.   

Abstract

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Year:  1995        PMID： 7646731      PMCID： PMC2550111          DOI： 10.1136/bmj.311.6996.58c

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  3 in total

1.  Genetic testing for familial hypertrophic cardiomyopathy in newborn infants.

Authors:  M P Ryan; J French; S al-Mahdawi; P Nihoyannopoulos; J G Cleland; C M Oakley; P S Harper; A Clarke; J Davis; L Grigg
Journal:  BMJ       Date:  1995-04-01

2.  DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study.

Authors:  H T Lynch; P Watson; T A Conway; J F Lynch; S M Slominski-Caster; S A Narod; J Feunteun; G Lenoir
Journal:  Arch Intern Med       Date:  1993-09-13

3.  The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing.

Authors:  S Wiggins; P Whyte; M Huggins; S Adam; J Theilmann; M Bloch; S B Sheps; M T Schechter; M R Hayden
Journal:  N Engl J Med       Date:  1992-11-12       Impact factor: 91.245
  3 in total
  3 in total

Review 1.  Neonatal screening for sickle cell disorders: what about the carrier infants?

Authors:  L Laird; C Dezateux; E N Anionwu
Journal:  BMJ       Date:  1996-08-17

2.  The genetic testing of children.

Authors:  A Fryer
Journal:  J R Soc Med       Date:  1997-08       Impact factor: 5.344

3.  Impediments to DNA testing and cascade screening for hypertrophic cardiomyopathy and Long QT syndrome: a qualitative study of patient experiences.

Authors:  Andrew Smart
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537
  3 in total

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