Cited by

• A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.

  Richard CW 3rd, Boehnke M, Berg DJ, Lichy JH, Meeker TC, Hauser E, Myers RM, Cox DR. Richard CW 3rd, et al. Am J Hum Genet. 1993 May;52(5):915-21. Am J Hum Genet. 1993. PMID: 8387721 Free PMC article.
• The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

  Kwiatkowski TJ Jr, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M, et al. Kwiatkowski TJ Jr, et al. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.
• Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

  Greger V, Knoll JH, Wagstaff J, Woolf E, Lieske P, Glatt H, Benn PA, Rosengren SS, Lalande M. Greger V, et al. Am J Hum Genet. 1997 Mar;60(3):574-80. Am J Hum Genet. 1997. PMID: 9042916 Free PMC article.
• Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes.

  Sirugo G, Keats B, Fujita R, Duclos F, Purohit K, Koenig M, Mandel JL. Sirugo G, et al. Am J Hum Genet. 1992 Mar;50(3):559-66. Am J Hum Genet. 1992. PMID: 1347194 Free PMC article.
• Molecular characterization of patients with 18q23 deletions.

  Strathdee G, Sutherland R, Jonsson JJ, Sataloff R, Kohonen-Corish M, Grady D, Overhauser J. Strathdee G, et al. Am J Hum Genet. 1997 Apr;60(4):860-8. Am J Hum Genet. 1997. PMID: 9106532 Free PMC article.