Feinberg AP - Search Results

1

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Alders M, et al. Among authors: feinberg ap. Am J Hum Genet. 2000 May;66(5):1473-84. doi: 10.1086/302892. Epub 2000 Apr 10. Am J Hum Genet. 2000. PMID: 10762538 Free PMC article.

2

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A. Mannens M, et al. Med Pediatr Oncol. 1996 Nov;27(5):490-4. doi: 10.1002/(SICI)1096-911X(199611)27:5<490::AID-MPO17>3.0.CO;2-E. Med Pediatr Oncol. 1996. PMID: 8827079 Review.

3

Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.

Alders M, Bliek J, Redeker B, Ryan A, Feinberg A, Westerveld A, Little P, Mannens M. Alders M, et al. Med Pediatr Oncol. 1996 Nov;27(5):495-7. doi: 10.1002/(SICI)1096-911X(199611)27:5<495::AID-MPO18>3.0.CO;2-9. Med Pediatr Oncol. 1996. PMID: 8827080 No abstract available.

4

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, Coad N, Steenman M, Bliek J, et al. Mannens M, et al. Among authors: feinberg ap. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

5

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP. Hoovers JM, et al. Among authors: feinberg ap. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12456-60. doi: 10.1073/pnas.92.26.12456. Proc Natl Acad Sci U S A. 1995. PMID: 8618920 Free PMC article.

6

TaqI and RsaI polymorphisms in the H19 gene (D11S813E).

Redeker E, Van Moorsel CJ, Feinberg A, Mannens M. Redeker E, et al. Hum Mol Genet. 1993 Jun;2(6):823. doi: 10.1093/hmg/2.6.823. Hum Mol Genet. 1993. PMID: 8102574 No abstract available.

7

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: feinberg ap. 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.

8

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.

Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR. Niemitz EL, et al. Among authors: feinberg ap. Am J Hum Genet. 2005 Nov;77(5):887-91. doi: 10.1086/497540. Epub 2005 Oct 3. Am J Hum Genet. 2005. PMID: 16252245 Free PMC article.

9

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

Paulsen M, Davies KR, Bowden LM, Villar AJ, Franck O, Fuermann M, Dean WL, Moore TF, Rodrigues N, Davies KE, Hu RJ, Feinberg AP, Maher ER, Reik W, Walter J. Paulsen M, et al. Among authors: feinberg ap. Hum Mol Genet. 1998 Jul;7(7):1149-59. doi: 10.1093/hmg/7.7.1149. Hum Mol Genet. 1998. PMID: 9618174

10

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. Among authors: feinberg ap. Am J Hum Genet. 1997 Aug;61(2):304-9. doi: 10.1086/514858. Am J Hum Genet. 1997. PMID: 9311734 Free PMC article.

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