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• Multipoint linkage analysis in Menkes disease.

  Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N. Tønnesen T, et al. Am J Hum Genet. 1992 May;50(5):1012-7. Am J Hum Genet. 1992. PMID: 1570830 Free PMC article.
• Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.

  Scheffer H, te Meerman GJ, Kruize YC, van den Berg AH, Penninga DP, Tan KE, der Kinderen DJ, Buys CH. Scheffer H, et al. Am J Hum Genet. 1989 Aug;45(2):252-60. Am J Hum Genet. 1989. PMID: 2569269 Free PMC article.
• Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.

  Yagle MK, Parruti G, Xu W, Ponder BA, Solomon E. Yagle MK, et al. Proc Natl Acad Sci U S A. 1990 Sep;87(18):7255-9. doi: 10.1073/pnas.87.18.7255. Proc Natl Acad Sci U S A. 1990. PMID: 2119504 Free PMC article.
• A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

  Tops CM, Breukel C, van der Klift HM, von Leeuwen IS, Wijnen JT, Griffioen G, Vasen HF, den Hartog Jager FC, Nagengast FM, Lamers CB, et al. Tops CM, et al. Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835. Hum Genet. 1991. PMID: 1671849
• X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci.

  Thomas NS, Williams H, Cole G, Roberts K, Clarke A, Liechti-Gallati S, Braga S, Gerber A, Meier C, Moser H, et al. Thomas NS, et al. J Med Genet. 1990 May;27(5):284-7. doi: 10.1136/jmg.27.5.284. J Med Genet. 1990. PMID: 2352256 Free PMC article.