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Items: 20

1.

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.

Lancet. 1991 Sep 7;338(8767):638-9. No abstract available.

PMID:
1679180
2.

[Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].

Pfeiffer RA, Tschech L, Irle U, Wündisch GF.

Klin Padiatr. 1987 Sep-Oct;199(5):329-35. Review. German.

PMID:
3316824
3.

Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.

Khan NL, Wood NW.

Curr Opin Neurol. 1999 Apr;12(2):149-54. Review.

PMID:
10226746
4.

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.

Cassidy SB, Schwartz S.

Medicine (Baltimore). 1998 Mar;77(2):140-51. Review.

5.

Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.

Casamassima AC, Shapiro LR, Wilmot PL, Smith KB.

Clin Genet. 1991 Apr;39(4):294-7. Review.

PMID:
1817468
6.

Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.

Nicholls RD, Ohta T, Gray TA.

Acta Paediatr Suppl. 1999 Dec;88(433):99-104. Review.

PMID:
10626556
7.

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.

Nicholls RD.

Am J Med Genet. 1993 Apr 1;46(1):16-25. Review.

PMID:
8388169
8.

Genomic imprinting and human chromosome 15.

Repetto GM.

Biol Res. 2001;34(2):141-5. Review.

PMID:
11715207
9.

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Kalsner L, Chamberlain SJ.

Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Review.

10.

Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.

Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.

Genet Couns. 1999;10(2):123-32. Review.

PMID:
10422004
11.

Prader-Willi syndrome and Angelman syndrome.

Buiting K.

Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):365-76. doi: 10.1002/ajmg.c.30273. Review.

PMID:
20803659
12.

Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).

Varela MC, Lopes GM, Koiffmann CP.

Ann Genet. 2004 Jul-Sep;47(3):267-73. Review.

PMID:
15337472
13.

Inv dup(15) supernumerary marker chromosomes.

Webb T.

J Med Genet. 1994 Aug;31(8):585-94. Review. No abstract available.

14.

[Genomic imprinting and its role in Prader-Willi and Angelman syndromes].

Mglinets VA, Levina LIa, Konstantinova LM.

Genetika. 1996 Dec;32(12):1605-15. Review. Russian.

PMID:
9102354
15.

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.

Knoll JH, Wagstaff J, Lalande M.

Am J Med Genet. 1993 Apr 1;46(1):2-6. Review.

PMID:
8388170
16.

Differentiated recurrence risk estimations in the Prader-Willi syndrome.

Kennerknecht I.

Clin Genet. 1992 Jun;41(6):303-8. Review.

PMID:
1623627
17.

Familial Prader-Willi syndrome: case report and a literature review.

McEntagart ME, Webb T, Hardy C, King MD.

Clin Genet. 2000 Sep;58(3):216-23. Review.

PMID:
11076044
18.

Genetic and clinical advances in Prader-Willi syndrome.

Wharton RH, Loechner KJ.

Curr Opin Pediatr. 1996 Dec;8(6):618-24. Review.

PMID:
9018447
19.

Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes.

Kelsey G, Reik W.

Bioessays. 1997 May;19(5):361-5. Review.

PMID:
9174400
20.

Genomic imprinting.

Hall JG.

Curr Opin Genet Dev. 1991 Jun;1(1):34-9. Review.

PMID:
1840876

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