Literature DB >> 5524819

[Segregation analysis of myotonia atrophica].

A Todorov, M Jéquier, D Klein, N E Morton.   

Abstract

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Year:  1970        PMID： 5524819

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  5 in total

1.  Genetic structure of Switzerland.

Authors:  N E Morton; D Klein; I E Hussels; P Dodinval; A Todorov; R Lew; S Yee
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

2.  Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.

Authors:  A E MacKenzie; H L MacLeod; A G Hunter; R G Korneluk
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

3.  Myotonia congenita and myotonic dystrophy: descriptive epidemiological investigation in Turin, Italy (1955-1979).

Authors:  L Pinessi; L Bergamini; R Cantello; C Di Tizio
Journal:  Ital J Neurol Sci       Date:  1982-10

4.  A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Authors:  K Johnson; P Shelbourne; J Davies; J Buxton; E Nimmo; M J Siciliano; L L Bachinski; M Anvret; H Harley; S Rundle
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

5.  Evidence for localization of the myotonic dystrophy protein kinase to the terminal cisternae of the sarcoplasmic reticulum.

Authors:  S Salvatori; D Biral; S Furlan; O Marin
Journal:  J Muscle Res Cell Motil       Date:  1997-08       Impact factor: 2.698
  5 in total

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