Korenberg JR - Search Results

1

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O. Giglio S, et al. Among authors: korenberg jr. Circulation. 2000 Jul 25;102(4):432-7. doi: 10.1161/01.cir.102.4.432. Circulation. 2000. PMID: 10908216

2

Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.

Botta A, Novelli G, Mari A, Novelli A, Sabani M, Korenberg J, Osborne LR, Digilio MC, Giannotti A, Dallapiccola B. Botta A, et al. J Med Genet. 1999 Jun;36(6):478-80. J Med Genet. 1999. PMID: 10874638 Free PMC article.

3

Down syndrome congenital heart disease: a narrowed region and a candidate gene.

Barlow GM, Chen XN, Shi ZY, Lyons GE, Kurnit DM, Celle L, Spinner NB, Zackai E, Pettenati MJ, Van Riper AJ, Vekemans MJ, Mjaatvedt CH, Korenberg JR. Barlow GM, et al. Among authors: korenberg jr. Genet Med. 2001 Mar-Apr;3(2):91-101. doi: 10.1097/00125817-200103000-00002. Genet Med. 2001. PMID: 11280955 Free article.

4

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG. Wu YQ, et al. Among authors: korenberg jr. Am J Med Genet. 1998 Jun 16;78(1):82-9. doi: 10.1002/(sici)1096-8628(19980616)78:1<82::aid-ajmg17>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9637430

5

Deletion of chromosome 21 disturbs human brain morphogenesis.

Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, Korenberg JR. Yao G, et al. Among authors: korenberg jr. Genet Med. 2006 Jan;8(1):1-7. doi: 10.1097/01.gim.0000195892.60506.3f. Genet Med. 2006. PMID: 16418593 Free article.

6

Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects.

Grossman TR, Gamliel A, Wessells RJ, Taghli-Lamallem O, Jepsen K, Ocorr K, Korenberg JR, Peterson KL, Rosenfeld MG, Bodmer R, Bier E. Grossman TR, et al. Among authors: korenberg jr. PLoS Genet. 2011 Nov;7(11):e1002344. doi: 10.1371/journal.pgen.1002344. Epub 2011 Nov 3. PLoS Genet. 2011. PMID: 22072978 Free PMC article.

7

Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion.

Korenberg JR, Kalousek DK, Anneren G, Pulst SM, Hall JG, Epstein CJ, Cox DR. Korenberg JR, et al. Hum Genet. 1991 Jun;87(2):112-8. doi: 10.1007/BF00204163. Hum Genet. 1991. PMID: 2066097

8

BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.

Hubert RS, Mitchell S, Chen XN, Ekmekji K, Gadomski C, Sun Z, Noya D, Kim UJ, Chen C, Shizuya H, Simon M, de Jong PJ, Korenberg JR. Hubert RS, et al. Among authors: korenberg jr. Genomics. 1997 Apr 15;41(2):218-26. doi: 10.1006/geno.1997.4657. Genomics. 1997. PMID: 9143497

9

A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

Wilson L, Curtis A, Korenberg JR, Schipper RD, Allan L, Chenevix-Trench G, Stephenson A, Goodship J, Burn J. Wilson L, et al. Among authors: korenberg jr. Am J Hum Genet. 1993 Dec;53(6):1262-8. Am J Hum Genet. 1993. PMID: 8250042 Free PMC article.

10

Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.

Korenberg JR, Bradley C, Disteche CM. Korenberg JR, et al. Am J Hum Genet. 1992 Feb;50(2):294-302. Am J Hum Genet. 1992. PMID: 1531166 Free PMC article.

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