Genetic anticipation and musculoskeletal disease.

In 1985, Strom et al described two families in which rheumatoid arthritis (RA) appeared in several members over three consecutive generations.' Although these pedigrees taken alone could implicate dominant inheritance, the overall picture with RA pedigrees indicates a complex mode of inheritance, with incomplete penetrance of predisposing genes and probably several genes being involved in the diseases process. In addition, an interesting observation in both pedigrees described by Strom's group and one which is difficult to understand in terms of classical Mendelian genetics is that the disease tended to

[1]  G. Thomson,et al.  Does genetic anticipation occur in familial rheumatoid arthritis? , 1994, Annals of the rheumatic diseases.

[2]  W. Honer,et al.  Evidence for anticipation in schizophrenia. , 1994, American journal of human genetics.

[3]  S H Moolgavkar,et al.  Allelic instability in mitosis: a unified model for dominant disorders. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[4]  W. Brown,et al.  Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. , 1993, American journal of human genetics.

[5]  P. Gregersen Discordance for autoimmunity in monozygotic twins. Are "identical" twins really identical? , 1993, Arthritis and rheumatism.

[6]  F. McMahon,et al.  Anticipation in bipolar affective disorder. , 1993, American journal of human genetics.

[7]  K. Dieckmann,et al.  HLA antigens, Lewis antigens, and blood groups in patients with testicular germ-cell tumors. , 1993, Oncology.

[8]  M. McInnis,et al.  Genes with triplet repeats: candidate mediators of neuropsychiatric disorders , 1993, Trends in Neurosciences.

[9]  Huda Y. Zoghbi,et al.  Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 , 1993, Nature Genetics.

[10]  W. Reardon,et al.  Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. , 1993, American journal of human genetics.

[11]  D. Nelson,et al.  Trinucleotide repeat instability: when and where? , 1993, Nature Genetics.

[12]  Manish S. Shah,et al.  A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes , 1993, Cell.

[13]  D. F. Roberts,et al.  Effect of disease severity on rheumatoid arthritis concordance in same sexed siblings. , 1992, Annals of the rheumatic diseases.

[14]  W. Reardon,et al.  Anticipation in myotonic dystrophy: new light on an old problem. , 1992, American journal of human genetics.

[15]  D. Nelson,et al.  Triplet repeat mutations in human disease. , 1992, Science.

[16]  R. Richards,et al.  Heritable unstable DNA sequences , 1992, Nature Genetics.

[17]  David E. Housman,et al.  Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member , 1992, Cell.

[18]  C. Amemiya,et al.  Cloning of the essential myotonic dystrophy region and mapping of the putative defect , 1992, Nature.

[19]  David E. Housman,et al.  Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy , 1992, Nature.

[20]  P. Jong,et al.  Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy , 1992, Nature.

[21]  K. Fischbeck,et al.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.

[22]  C. Deighton,et al.  The familial nature of rheumatoid arthritis. , 1991, Annals of the rheumatic diseases.

[23]  A. Silman,et al.  Review of UK data on the rheumatic diseases--2. Rheumatoid arthritis. , 1990, British journal of rheumatology.

[24]  A. Silman,et al.  Failure to find disease similarity in sibling pairs with rheumatoid arthritis. , 1987, Annals of the rheumatic diseases.