The use of genetic linkage in counselling families with dystrophia myotonica-Reference-Cited by-同舟云学术

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The use of genetic linkage in counselling families with dystrophia myotonica

Published:2008-04-23 Issue:6 Volume:17 Page:443-448
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Gibson Sheila L. M.,Ferguson-Smith M. A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb00178.x/fullpdf

Reference15 articles.

1. Early recognition of heterozygotes for the gene for dystrophia myotonica;Bundey;J. Neurol. Neurosurg. Psychiat.,1970

2. Gibson , S. L. M. M.A. Ferguson-Smith The secretor status of the foetus

3. Pre-symptomatic detection and genetic counselling in myotonic dystrophy;Harper;Clin. Genet.,1973

4. ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis;Harper;J. med. Genet.,1971

5. Early onset dystrophia myotonica. Evidence supporting a maternal environmental factor;Harper;Lancet,1972

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The secretor status of the foetus;Clinical Genetics;2008-04-23

2. Congenital Myotonic Dystrophy.;Acta Paediatrica;1986-09

3. Myotonic Dystrophy and Pregnancy;The Australian and New Zealand Journal of Obstetrics and Gynaecology;1981-11

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