Debaun MR - Search Results

1

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.

Chang AS, Moley KH, Wangler M, Feinberg AP, Debaun MR. Chang AS, et al. Among authors: debaun mr. Fertil Steril. 2005 Feb;83(2):349-54. doi: 10.1016/j.fertnstert.2004.07.964. Fertil Steril. 2005. PMID: 15705373 Free PMC article.

2

Genomic imprinting, DNA methylation, and cancer.

Feinberg AP, Rainier S, DeBaun MR. Feinberg AP, et al. Among authors: debaun mr. J Natl Cancer Inst Monogr. 1995;(17):21-6. J Natl Cancer Inst Monogr. 1995. PMID: 8573447 Review. No abstract available.

3

Reduced expression of the cyclin-dependent kinase inhibitor gene p57KIP2 in Wilms' tumor.

Thompson JS, Reese KJ, DeBaun MR, Perlman EJ, Feinberg AP. Thompson JS, et al. Among authors: debaun mr. Cancer Res. 1996 Dec 15;56(24):5723-7. Cancer Res. 1996. PMID: 8971182

4

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.

Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP. Lee MP, et al. Am J Hum Genet. 1997 Aug;61(2):304-9. doi: 10.1086/514858. Am J Hum Genet. 1997. PMID: 9311734 Free PMC article.

5

Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome.

Choyke PL, Siegel MJ, Oz O, Sotelo-Avila C, DeBaun MR. Choyke PL, et al. Among authors: debaun mr. AJR Am J Roentgenol. 1998 Sep;171(3):733-7. doi: 10.2214/ajr.171.3.9725306. AJR Am J Roentgenol. 1998. PMID: 9725306

6

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP. Lee MP, et al. Among authors: debaun mr. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5203-8. doi: 10.1073/pnas.96.9.5203. Proc Natl Acad Sci U S A. 1999. PMID: 10220444 Free PMC article.

7

Hypoglycemia in Beckwith-Wiedemann syndrome.

DeBaun MR, King AA, White N. DeBaun MR, et al. Semin Perinatol. 2000 Apr;24(2):164-71. doi: 10.1053/sp.2000.6366. Semin Perinatol. 2000. PMID: 10805171 Review.

8

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.

DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP. DeBaun MR, et al. Am J Hum Genet. 2002 Mar;70(3):604-11. doi: 10.1086/338934. Epub 2002 Jan 28. Am J Hum Genet. 2002. PMID: 11813134 Free PMC article.

9

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.

DeBaun MR, Niemitz EL, Feinberg AP. DeBaun MR, et al. Am J Hum Genet. 2003 Jan;72(1):156-60. doi: 10.1086/346031. Epub 2002 Nov 18. Am J Hum Genet. 2003. PMID: 12439823 Free PMC article.

10

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.

Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP. Niemitz EL, et al. Among authors: debaun mr. Am J Hum Genet. 2004 Nov;75(5):844-9. doi: 10.1086/425343. Epub 2004 Sep 15. Am J Hum Genet. 2004. PMID: 15372379 Free PMC article.

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