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Case Reports

. 1991 Nov 16;338(8777):1276.

doi: 10.1016/0140-6736(91)92145-r.

Molecular cytogenetics of Prader-Willi and Angelman syndromes

M G Butler, M A Greenstein

PMID: 1682673
PMCID: PMC5493389
DOI: 10.1016/0140-6736(91)92145-r

Case Reports

Molecular cytogenetics of Prader-Willi and Angelman syndromes

M G Butler et al. Lancet. 1991.

. 1991 Nov 16;338(8777):1276.

doi: 10.1016/0140-6736(91)92145-r.

Authors

M G Butler, M A Greenstein

PMID: 1682673
PMCID: PMC5493389
DOI: 10.1016/0140-6736(91)92145-r

No abstract available

PubMed Disclaimer

Comment in

Molecular cytogenetics of Prader-Willi and Angelman syndromes.
Hultén M, Hardy G, Gould C, Stergianou R, Waters J, McKeown C. Hultén M, et al. Lancet. 1992 Jan 25;339(8787):243-4. doi: 10.1016/0140-6736(92)90043-3. Lancet. 1992. PMID: 1346195 No abstract available.

Comment on

Genomic imprinting in an Angelman and Prader-Willi translocation family.
Hultén M, Armstrong S, Challinor P, Gould C, Hardy G, Leedham P, Lee T, McKeown C. Hultén M, et al. Lancet. 1991 Sep 7;338(8767):638-9. doi: 10.1016/0140-6736(91)90652-6. Lancet. 1991. PMID: 1679180 No abstract available.

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Molecular cytogenetics of Prader-Willi and Angelman syndromes.
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Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?
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The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7.
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Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L, Chamberlain SJ. Kalsner L, et al. Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Pediatr Clin North Am. 2015. PMID: 26022164 Free PMC article. Review.

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Cited by

Molecular study of chromosome 15 in 22 patients with Angelman syndrome.
Beuten J, Mangelschots K, Buntinx I, Coucke P, Brouwer OF, Hennekam RC, Van Broeckhoven C, Willems PJ. Beuten J, et al. Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446. Hum Genet. 1993. PMID: 8094063
Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?
Butler MG. Butler MG. Am J Med Genet. 1994 Mar 1;50(1):42-5. doi: 10.1002/ajmg.1320500109. Am J Med Genet. 1994. PMID: 8160752 Free PMC article. No abstract available.
High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome.
Butler MG. Butler MG. Am J Med Genet. 1995 May 8;56(4):420-2. doi: 10.1002/ajmg.1320560414. Am J Med Genet. 1995. PMID: 7604853 Free PMC article. No abstract available.

References

1. Butler MG, Palmer CG. Parental origin of chromosome 15 deletion in Prader-Willi syndrome. Lancet. 1983;ii:1285–86. - PMC - PubMed
1. Knoll JHM, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA. Angelman and Prader-Willi syndrome share a common chromosome 15 deletion, but differ in parental origin of the deletion. Am J Med Genet. 1989;32:285–90. - PubMed

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