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Journal Abstract Search

383 related items for PubMed ID: 8609225

  • 21.
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  • 23. Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).
    Milunsky J, Huang XL, Baldwin CT, Farah MG, Milunsky A.
    Cancer Genet Cytogenet; 1998 Oct 15; 106(2):173-6. PubMed ID: 9797786
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  • 28. Radiation hybrid mapping of chromosomal region 2p15-p16: integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci.
    Taymans SE, Kirschner LS, Giatzakis C, Stratakis CA.
    Genomics; 1999 Mar 15; 56(3):344-9. PubMed ID: 10087203
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  • 30. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B.
    Neurology; 2007 Jun 12; 68(24):2107-12. PubMed ID: 17377072
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  • 31. A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.
    Khaliq S, Hameed A, Ismail M, Anwar K, Mehdi SQ.
    Invest Ophthalmol Vis Sci; 2002 Jul 12; 43(7):2083-7. PubMed ID: 12091400
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  • 33. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE, Ritch R, Lichter PR, Rozsa FW, Stringham HM, Caronia RM, Johnson D, Abundo GP, Willcockson J, Downs CA, Thompson DA, Musarella MA, Gupta N, Othman MI, Torrez DM, Herman SB, Wong DJ, Higashi M, Boehnke M.
    Ophthalmology; 1998 Sep 12; 105(9):1698-707. PubMed ID: 9754180
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  • 34. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
    Jiao X, Ritter R, Hejtmancik JF, Edwards AO.
    Invest Ophthalmol Vis Sci; 2004 Dec 12; 45(12):4498-503. PubMed ID: 15557460
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  • 35. Epithelioid blue nevus and psammomatous melanotic schwannoma: the unusual pigmented skin tumors of the Carney complex.
    Carney JA, Stratakis CA.
    Semin Diagn Pathol; 1998 Aug 12; 15(3):216-24. PubMed ID: 9711672
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  • 36. Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes.
    Kirschner LS, Taymans SE, Pack S, Pak E, Pike BL, Chandrasekharappa SC, Zhuang Z, Stratakis CA.
    Genomics; 1999 Nov 15; 62(1):21-33. PubMed ID: 10585764
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  • 37. Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).
    Stratakis CA, Lin JP, Rennert OM.
    Am J Med Genet; 1998 Sep 23; 79(3):209-14. PubMed ID: 9788564
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  • 38.
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  • 39. [PRKAR1A gene mutations in two patients with myxoma syndrome (Carney complex)].
    Skamrov AV, Feoktistova ES, Khaspekov GL, Kovalevskiĭ DA, Goriunova LE, Bibilashvili RSh, Vinnitskiĭ LI, Sheremet'eva GF, Nechaenko MA.
    Kardiologiia; 2003 Sep 23; 43(7):77-82. PubMed ID: 12891303
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  • 40. The significance of multiple, recurrent, and "complex" cardiac myxomas.
    McCarthy PM, Piehler JM, Schaff HV, Pluth JR, Orszulak TA, Vidaillet HJ, Carney JA.
    J Thorac Cardiovasc Surg; 1986 Mar 23; 91(3):389-96. PubMed ID: 3951243
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