DeBaun MR - Search Results

1

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.

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

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.

6

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.

7

Screening for cancer in children with Costello syndrome.

DeBaun MR. DeBaun MR. Am J Med Genet. 2002 Feb 15;108(1):88-90. doi: 10.1002/ajmg.10242. Am J Med Genet. 2002. PMID: 11857557 No abstract available.

8

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.

9

LIT1 and H19 methylation defects in isolated hemihyperplasia.

Martin RA, Grange DK, Zehnbauer B, Debaun MR. Martin RA, et al. Among authors: debaun mr. Am J Med Genet A. 2005 Apr 15;134A(2):129-31. doi: 10.1002/ajmg.a.30578. Am J Med Genet A. 2005. PMID: 15651076

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

444 results

Search Page

Filters