Literature DB >> 8024254

4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy.

G C Deidda, S Cacurri, I La Cesa, C Scoppetta, L Felicetti.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1994        PMID： 8024254     DOI： 10.1002/ana.410360128

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


× No keyword cloud information.
  3 in total

Review 1.  The muscular dystrophies: from genes to therapies.

Authors:  Richard M Lovering; Neil C Porter; Robert J Bloch
Journal:  Phys Ther       Date:  2005-12

2.  Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).

Authors:  G Deidda; S Cacurri; N Piazzo; L Felicetti
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

3.  Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy.

Authors:  S Cacurri; N Piazzo; G Deidda; E Vigneti; G Galluzzi; L Colantoni; B Merico; E Ricci; L Felicetti
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.