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Journal Abstract Search

153 related items for PubMed ID: 9500556

  • 1. Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22.
    Peters JM, Barnes R, Bennett L, Gitomer WM, Bowcock AM, Garg A.
    Nat Genet; 1998 Mar; 18(3):292-5. PubMed ID: 9500556
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  • 2. Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22.
    Anderson JL, Khan M, David WS, Mahdavi Z, Nuttall FQ, Krech E, West SG, Vance JM, Pericak-Vance MA, Nance MA.
    Am J Med Genet; 1999 Jan 15; 82(2):161-5. PubMed ID: 9934982
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  • 4. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.
    Garg A, Wilson R, Barnes R, Arioglu E, Zaidi Z, Gurakan F, Kocak N, O'Rahilly S, Taylor SI, Patel SB, Bowcock AM.
    J Clin Endocrinol Metab; 1999 Sep 15; 84(9):3390-4. PubMed ID: 10487716
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  • 6. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 15; 152(1):29-36. PubMed ID: 15656797
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  • 7. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
    Magré J, Delépine M, Khallouf E, Gedde-Dahl T, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon-Chevalier A, Polak M, Robert JJ, Tric P, Tubiana-Rufi N, Vigouroux C, Weissenbach J, Savasta S, Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J, BSCL Working Group.
    Nat Genet; 2001 Aug 15; 28(4):365-70. PubMed ID: 11479539
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  • 8. Phenotypic gender differences in subjects with familial partial lipodystrophy (Dunnigan variety) due to a nuclear lamin A/C R482W mutation.
    Araújo-Vilar D, Loidi L, Domínguez F, Cabezas-Cerrato J.
    Horm Metab Res; 2003 Jan 15; 35(1):29-35. PubMed ID: 12669268
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  • 9. Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.
    Weyer C, Wolford JK, Hanson RL, Foley JE, Tataranni PA, Bogardus C, Pratley RE.
    Mol Genet Metab; 2001 Mar 15; 72(3):231-8. PubMed ID: 11243729
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  • 10. Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family.
    Kamatani N, Moritani M, Yamanaka H, Takeuchi F, Hosoya T, Itakura M.
    Arthritis Rheum; 2000 Apr 15; 43(4):925-9. PubMed ID: 10765940
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  • 11. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
    Orenstein SR, Shalaby TM, Finch R, Pfuetzer RH, DeVandry S, Chensny LJ, Bannada MM, Whitcomb DC.
    Am J Gastroenterol; 2002 Nov 15; 97(11):2725-32. PubMed ID: 12425539
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  • 12. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.
    Eur J Hum Genet; 2006 Mar 15; 14(3):340-8. PubMed ID: 16391564
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  • 13. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
    Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, Singh BM, Schmidt H, Brabant G, Kumar S, Durrington PN, Gregory S, O'Rahilly S, Trembath RC.
    Nat Genet; 2000 Feb 15; 24(2):153-6. PubMed ID: 10655060
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  • 14. Linkage of body mass index to chromosome 20 in Utah pedigrees.
    Hunt SC, Abkevich V, Hensel CH, Gutin A, Neff CD, Russell DL, Tran T, Hong X, Jammulapati S, Riley R, Weaver-Feldhaus J, Macalma T, Richards MM, Gress R, Francis M, Thomas A, Frech GC, Adams TD, Shattuck D, Stone S.
    Hum Genet; 2001 Sep 15; 109(3):279-85. PubMed ID: 11702208
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  • 15. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.
    Br J Ophthalmol; 2005 Jul 15; 89(7):831-4. PubMed ID: 15965161
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  • 16. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
    Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F.
    Nephrol Dial Transplant; 2005 May 15; 20(5):909-14. PubMed ID: 15741201
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