Literature DB >> 6214632

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

P S Harper, A Tyler, S Smith, P Jones, R G Newcombe, V McBroom.   

Abstract

A regional genetic register for Huntington's chorea in South Wales is described, based on previous family studies in this area, which is one of high prevalence for the disorder. The primary role of the register is to help in the efficient delivery of services, including genetic counselling, to affected subjects and relatives, and to monitor changes in the population at risk. The mode of operation of the register is described and the essential importance of strict confidentiality is stressed.

Entities:  

Mesh：

Year:  1982        PMID： 6214632      PMCID： PMC1048888          DOI： 10.1136/jmg.19.4.241

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


  5 in total

1.  A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party.

Authors:  A E Emery; C Brough; M Crawfurd; P Harper; R Harris; G Oakshott
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

2.  Decline in the predicted incidence of Huntington's chorea associated with systematic genetic counselling and family support.

Authors:  P S Harper; A Tyler; S Smith; P Jones; R G Newcombe; V McBroom
Journal:  Lancet       Date:  1981-08-22       Impact factor: 79.321

3.  A life table for onset of Huntington's chorea.

Authors:  R G Newcombe
Journal:  Ann Hum Genet       Date:  1981-10       Impact factor: 1.670

4.  Huntington's Chorea in South Wales. A genetic and epidemiological study.

Authors:  D A Walker; P S Harper; C E Wells; A Tyler; K Davies; R G Newcombe
Journal:  Clin Genet       Date:  1981-04       Impact factor: 4.438

5.  Huntington's chorea. The basis for long-term prevention.

Authors:  P S Harper; D A Walker; A Tyler; R G Newcombe; K Davies
Journal:  Lancet       Date:  1979-08-18       Impact factor: 79.321
  5 in total
  5 in total

1.  Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.

Authors:  P S Harper; S Youngman; M A Anderson; M Sarfarazi; O Quarrell; R Tanzi; D Shaw; P Wallace; P M Conneally; J F Gusella
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

2.  Genetic prediction and family structure in Huntington's chorea.

Authors:  P S Harper; M Sarfarazi
Journal:  Br Med J (Clin Res Ed)       Date:  1985-06-29

3.  Molecular genetics in clinical practice: evolution of a DNA diagnostic service.

Authors:  A L Meredith; M Upadhyaya; P S Harper
Journal:  BMJ       Date:  1988-10-01

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

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

5.  Population based study of late onset cerebellar ataxia in south east Wales.

Authors:  M B Muzaimi; J Thomas; S Palmer-Smith; L Rosser; P S Harper; C M Wiles; D Ravine; N P Robertson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-08       Impact factor: 10.154
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.