Research Article

Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion†

  1. Sarah L. Nolin*,
  2. Xiao-hua Ding,
  3. George E. Houck,
  4. W. Ted Brown,
  5. Carl Dobkin

Article first published online: 11 DEC 2007

DOI: 10.1002/ajmg.a.32087

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 1, pages 60–65, 1 January 2008

Additional Information

How to Cite

Nolin, S. L., Ding, X.-h., Houck, G. E., Brown, W. T. and Dobkin, C. (2008), Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion. Am. J. Med. Genet., 146A: 60–65. doi: 10.1002/ajmg.a.32087

Author Information

  1. New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York

*NYS Institute for Basic Research, Human Genetics Department, 1050 Forest Hill Road, Staten Island, NY 10314.

  1. †

    How to cite this article: Nolin SL, Ding X-h, Houck GE, Brown WT, Dobkin C. 2007. Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion. Am J Med Genet Part A 146A:60–65.

Publication History

  1. Issue published online: 19 DEC 2007
  2. Article first published online: 11 DEC 2007
  3. Manuscript Accepted: 23 AUG 2007
  4. Manuscript Received: 11 APR 2007

Funded by

  • New York State Office of Mental Retardation and Developmental Disabilities

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