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Literature DB >> 7864684

Genetic anticipation and musculoskeletal disease.

C M Deighton¹, G Thomson.

Abstract

Entities: Disease

Mesh：

Year: 1994 PMID： 7864684 PMCID： PMC1005471 DOI： 10.1136/ard.53.12.787

Source DB: PubMed Journal: Ann Rheum Dis ISSN： 0003-4967 Impact factor: 19.103

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25 in total

1. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

Authors: A R La Spada; E M Wilson; D B Lubahn; A E Harding; K H Fischbeck
Journal: Nature Date: 1991-07-04 Impact factor: 49.962

Review 2. The familial nature of rheumatoid arthritis.

Authors: C M Deighton; D J Walker
Journal: Ann Rheum Dis Date: 1991-01 Impact factor: 19.103

Review 3. Triplet repeat mutations in human disease.

Authors: C T Caskey; A Pizzuti; Y H Fu; R G Fenwick; D L Nelson
Journal: Science Date: 1992-05-08 Impact factor: 47.728

4. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors: A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal: Cell Date: 1991-05-31 Impact factor: 41.582

5. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Authors: H G Harley; J D Brook; S A Rundle; S Crow; W Reardon; A J Buckler; P S Harper; D E Housman; D J Shaw
Journal: Nature Date: 1992-02-06 Impact factor: 49.962

6. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

Authors: J Buxton; P Shelbourne; J Davies; C Jones; T Van Tongeren; C Aslanidis; P de Jong; G Jansen; M Anvret; B Riley
Journal: Nature Date: 1992-02-06 Impact factor: 49.962

7. Cloning of the essential myotonic dystrophy region and mapping of the putative defect.

Authors: C Aslanidis; G Jansen; C Amemiya; G Shutler; M Mahadevan; C Tsilfidis; C Chen; J Alleman; N G Wormskamp; M Vooijs
Journal: Nature Date: 1992-02-06 Impact factor: 49.962

8. Failure to find disease similarity in sibling pairs with rheumatoid arthritis.

Authors: A J Silman; W E Ollier; H L Currey
Journal: Ann Rheum Dis Date: 1987-02 Impact factor: 19.103

9. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors: J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal: Cell Date: 1992-02-21 Impact factor: 41.582