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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. Among authors: chorney m, chorney k. 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.
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: chorney mj. Am J Med Genet. 1993 Jul 1;46(6):623-9. doi: 10.1002/ajmg.1320460604. Am J Med Genet. 1993. PMID: 8103286
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. Among authors: chorney ka, chorney mj. 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.
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: chorney ka, chorney m. 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.
74 results