Literature DB >> 4861055

[Progressive muscle dystrophy. 8. Occurrence, clinical aspects and genetics of types I and II].

H Moser, U Wiesmann, R Richterich, E Rossi.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1966        PMID： 4861055

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


× No keyword cloud information.
  3 in total

Review 1.  [New data on the genetics and classification of muscular dystrophies].

Authors:  P E Becker
Journal:  Humangenetik       Date:  1972

2.  Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B.

Authors:  J R Gilbert; M C Speer; J Stajich; R Clancy; K Lewis; H Qiu; L Yamaoka; A Kumar; J Vance; C Stewart
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

3.  Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD).

Authors:  J R Gilbert; J M Stajich; S Wall; S C Carter; H Qiu; J M Vance; C S Stewart; M C Speer; J Pufky; L H Yamaoka
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.