Venditti CP - Search Results

1

Mutation analysis in hereditary hemochromatosis.

Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Ten Elshof AE, Gerhard GS, Chorney M. Beutler E, et al. Among authors: venditti cp. Blood Cells Mol Dis. 1996;22(2):187-94; discussion 194a-194b. doi: 10.1006/bcmd.1996.0027. Blood Cells Mol Dis. 1996. PMID: 8931958 Free article.

2

Localization of the hemochromatosis disease gene: linkage disequilibrium analysis using an American patient collection.

Seese NK, Venditti CP, Chorney KA, Gerhard GS, Ma J, Hudson TJ, Phatak PD, Chorney MJ. Seese NK, et al. Among authors: venditti cp. Blood Cells Mol Dis. 1996;22(1):36-46; discussion 47-8. doi: 10.1006/bcmd.1996.0006. Blood Cells Mol Dis. 1996. PMID: 8807084 Free article.

3

46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.

Venditti CP, Seese NK, Gerhard GS, Ten Elshof AE, Chorney KA, Mowrey PN, Lacey PG, Knoll JH, Chorney MJ. Venditti CP, et al. J Med Genet. 1997 Jan;34(1):24-7. doi: 10.1136/jmg.34.1.24. J Med Genet. 1997. PMID: 9032645 Free PMC article.

4

Class I gene contraction within the HLA-A subregion of the human MHC.

Venditti CP, Chorney MJ. Venditti CP, et al. Genomics. 1992 Dec;14(4):1003-9. doi: 10.1016/s0888-7543(05)80123-5. Genomics. 1992. PMID: 1362179

5

Mapping and characterization of non-HLA multigene assemblages in the human MHC class I region.

Venditti CP, Harris JM, Geraghty DE, Chorney MJ. Venditti CP, et al. Genomics. 1994 Jul 15;22(2):257-66. doi: 10.1006/geno.1994.1382. Genomics. 1994. PMID: 7806210

6

DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) Project.

Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Venditti CP, Kasarda S, Thompson LA, Detterman DK, et al. Plomin R, et al. Among authors: venditti cp. Behav Genet. 1994 Mar;24(2):107-18. doi: 10.1007/BF01067815. Behav Genet. 1994. PMID: 8024528

7

Structure and content of the major histocompatibility complex (MHC) class I regions of the great anthropoid apes.

Venditti CP, Lawlor DA, Sharma P, Chorney MJ. Venditti CP, et al. Hum Immunol. 1996 Sep 1;49(2):71-84. doi: 10.1016/0198-8859(96)00017-1. Hum Immunol. 1996. PMID: 8872161

8

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Drumheller T, McGillivray BC, Behrner D, MacLeod P, McFadden DE, Roberson J, Venditti C, Chorney K, Chorney M, Smith DI. Drumheller T, et al. J Med Genet. 1996 Oct;33(10):842-7. doi: 10.1136/jmg.33.10.842. J Med Genet. 1996. PMID: 8933338 Free PMC article.

9

Studies of the 6.7 family of dispersed genomic fragments within the MHC class I Region.

Pichon L, Venditti C, Harris J, Ten Elshof A, Pinelli M, Chorney M. Pichon L, et al. Exp Clin Immunogenet. 1997;14(2):131-40. Exp Clin Immunogenet. 1997. PMID: 9395889

10

Clinical and molecular analyses of deletion 3p25-pter syndrome.

Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL. Mowrey PN, et al. Among authors: venditti cp. Am J Med Genet. 1993 Jul 1;46(6):623-9. doi: 10.1002/ajmg.1320460604. Am J Med Genet. 1993. PMID: 8103286

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