Noll WW - Search Results

1

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

Mohandas TK, Park JP, Spellman RA, Filiano JJ, Mamourian AC, Hawk AB, Belloni DR, Noll WW, Moeschler JB. Mohandas TK, et al. Among authors: noll ww. Am J Med Genet. 1999 Feb 12;82(4):294-300. Am J Med Genet. 1999. PMID: 10051161

2

Estimate of prevalence of proximal 15q duplication syndrome.

Moeschler JB, Mohandas TK, Hawk AB, Noll WW. Moeschler JB, et al. Among authors: noll ww. Am J Med Genet. 2002 Sep 1;111(4):440-2. doi: 10.1002/ajmg.10419. Am J Med Genet. 2002. PMID: 12210307 No abstract available.

3

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).

Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK. Park JP, et al. Among authors: noll ww. Am J Med Genet. 1998 Jun 30;78(2):134-9. Am J Med Genet. 1998. PMID: 9674903

4

Amplification of the MLL region in acute myeloid leukemia.

Park JP, Ladd SL, Ely P, Weiner NJ, Wojiski SA, Hawk AB, Noll WW, Mohandas TK. Park JP, et al. Among authors: noll ww. Cancer Genet Cytogenet. 2000 Sep;121(2):198-205. doi: 10.1016/s0165-4608(00)00256-9. Cancer Genet Cytogenet. 2000. PMID: 11063808

5

Constitutional de novo t(1;22)(p22;q11.2) and ependymoma.

Park JP, Chaffee S, Noll WW, Rhodes CH. Park JP, et al. Among authors: noll ww. Cancer Genet Cytogenet. 1996 Feb;86(2):150-2. doi: 10.1016/0165-4608(95)00182-4. Cancer Genet Cytogenet. 1996. PMID: 8603343

6

Human acyl-CoA:cholesterol acyltransferase-1 (ACAT-1) gene organization and evidence that the 4.3-kilobase ACAT-1 mRNA is produced from two different chromosomes.

Li BL, Li XL, Duan ZJ, Lee O, Lin S, Ma ZM, Chang CC, Yang XY, Park JP, Mohandas TK, Noll W, Chan L, Chang TY. Li BL, et al. J Biol Chem. 1999 Apr 16;274(16):11060-71. doi: 10.1074/jbc.274.16.11060. J Biol Chem. 1999. PMID: 10196189 Free article.

7

Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoter.

Noll WW, Belloni DR, Rutter JL, Storm CA, Schned AR, Titus-Ernstoff L, Ernstoff MS, Brinckerhoff CE. Noll WW, et al. Am J Pathol. 2001 Feb;158(2):691-7. doi: 10.1016/S0002-9440(10)64011-4. Am J Pathol. 2001. PMID: 11159206 Free PMC article.

8

Tampon samplings with longer cervicovaginal cell exposures are equivalent to two consecutive swabs for the detection of high-risk human papillomavirus.

Harper DM, Raymond M, Noll WW, Belloni DR, Duncan LT, Cole BF. Harper DM, et al. Among authors: noll ww. Sex Transm Dis. 2002 Nov;29(11):628-36. doi: 10.1097/00007435-200211000-00003. Sex Transm Dis. 2002. PMID: 12438897 Clinical Trial.

9

Randomized clinical trial of PCR-determined human papillomavirus detection methods: self-sampling versus clinician-directed--biologic concordance and women's preferences.

Harper DM, Noll WW, Belloni DR, Cole BF. Harper DM, et al. Among authors: noll ww. Am J Obstet Gynecol. 2002 Mar;186(3):365-73. doi: 10.1067/mob.2002.121076. Am J Obstet Gynecol. 2002. PMID: 11904593 Clinical Trial.

10

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.

Noll WW, Belloni DR, Stenzel TT, Grody WW. Noll WW, et al. Nat Genet. 1999 Nov;23(3):271-2. doi: 10.1038/15722. Nat Genet. 1999. PMID: 10610176 No abstract available.

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