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Comment
. 1994 Mar 1;50(1):42-5.
doi: 10.1002/ajmg.1320500109.

Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?

M G Butler
Comment

Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?

M G Butler. Am J Med Genet. .
No abstract available

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Comment on

  • Cytogenetic and molecular analysis in Angelman syndrome.
    Zackowski JL, Nicholls RD, Gray BA, Bent-Williams A, Gottlieb W, Harris PJ, Waters MF, Driscoll DJ, Zori RT, Williams CA. Zackowski JL, et al. Am J Med Genet. 1993 Apr 1;46(1):7-11. doi: 10.1002/ajmg.1320460104. Am J Med Genet. 1993. PMID: 8098583

References

    1. Butler MG, Dahir GA, Schwartz HS. Molecular analysis of transforming growth factor beta in giant cell tumor of bone. Cancer Genet Cytogenet. 1993;66:108–112. - PMC - PubMed
    1. Butler MG, Greenstein MA. Molecular cytogenetics of Prader-Willi and Angelman syndromes. Lancet. 1991;338:1276. - PMC - PubMed
    1. Butler MG, Meaney FJ, Palmer CG. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. Am J Med Genet. 1986;23:793–809. - PMC - PubMed
    1. Butler MG, Palmer CG. Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet. 1983;1:1285–1286. - PMC - PubMed
    1. Mascari MJ, Ladda RL, Gottlieb W, Butler MG, Rogan PK, Armour J, Jeffreys A, Waller D, Nicholls RD. Molecular diagnosis in Prader-Willi syndrome identifies a common occurrence of maternal uniparental disomy. N Engl J Med. 1992;326:1599–1607. - PMC - PubMed

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