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Journal Abstract Search

224 related items for PubMed ID: 15322984

  • 1. Mutation history of the roma/gypsies.
    Morar B, Gresham D, Angelicheva D, Tournev I, Gooding R, Guergueltcheva V, Schmidt C, Abicht A, Lochmuller H, Tordai A, Kalmar L, Nagy M, Karcagi V, Jeanpierre M, Herczegfalvi A, Beeson D, Venkataraman V, Warwick Carter K, Reeve J, de Pablo R, Kucinskas V, Kalaydjieva L.
    Am J Hum Genet; 2004 Oct; 75(4):596-609. PubMed ID: 15322984
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  • 2. Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolates.
    Bouwer S, Angelicheva D, Chandler D, Seeman P, Tournev I, Kalaydjieva L.
    Genet Test; 2007 Oct; 11(4):455-8. PubMed ID: 18294064
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  • 3. A newly discovered founder population: the Roma/Gypsies.
    Kalaydjieva L, Morar B, Chaix R, Tang H.
    Bioessays; 2005 Oct; 27(10):1084-94. PubMed ID: 16163730
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  • 4. Origins and divergence of the Roma (gypsies).
    Gresham D, Morar B, Underhill PA, Passarino G, Lin AA, Wise C, Angelicheva D, Calafell F, Oefner PJ, Shen P, Tournev I, de Pablo R, Kuĉinskas V, Perez-Lezaun A, Marushiakova E, Popov V, Kalaydjieva L.
    Am J Hum Genet; 2001 Dec; 69(6):1314-31. PubMed ID: 11704928
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  • 7. The Consequence of a Founder Effect: CCR5-∆32, CCR2-64I and SDF1-3'A Polymorphism in Vlach Gypsy Population in Hungary.
    Juhász E, Béres J, Kanizsai S, Nagy K.
    Pathol Oncol Res; 2012 Apr; 18(2):177-82. PubMed ID: 21667221
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  • 8. A genetic historical sketch of European Gypsies: The perspective from autosomal markers.
    Gusmão A, Valente C, Gomes V, Alves C, Amorim A, Prata MJ, Gusmão L.
    Am J Phys Anthropol; 2010 Apr; 141(4):507-14. PubMed ID: 19918999
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  • 10. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
    Kalaydjieva L, Hallmayer J, Chandler D, Savov A, Nikolova A, Angelicheva D, King RH, Ishpekova B, Honeyman K, Calafell F, Shmarov A, Petrova J, Turnev I, Hristova A, Moskov M, Stancheva S, Petkova I, Bittles AH, Georgieva V, Middleton L, Thomas PK.
    Nat Genet; 1996 Oct; 14(2):214-7. PubMed ID: 8841199
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  • 15. Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.
    Sivadorai P, Cherninkova S, Bouwer S, Kamenarova K, Angelicheva D, Seeman P, Hollingsworth K, Mihaylova V, Oscar A, Dimitrova G, Kaneva R, Tournev I, Kalaydjieva L.
    Clin Genet; 2008 Jul; 74(1):82-7. PubMed ID: 18537981
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  • 16. Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families.
    Fiore M, Pillois X, Nurden P, Nurden AT, Austerlitz F.
    Eur J Hum Genet; 2011 Sep; 19(9):981-7. PubMed ID: 21487445
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  • 18. C283Y gamma-sarcoglycan gene mutation in the Bulgarian Roma (Gypsy) population: prevalence study and carrier screening in a high-risk community.
    Georgieva B, Todorova A, Tournev I, Mitev V, Kremensky I.
    Clin Genet; 2004 Nov; 66(5):467-72. PubMed ID: 15479193
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  • 20. Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.
    Diaz GA, Gelb BD, Risch N, Nygaard TG, Frisch A, Cohen IJ, Miranda CS, Amaral O, Maire I, Poenaru L, Caillaud C, Weizberg M, Mistry P, Desnick RJ.
    Am J Hum Genet; 2000 Jun; 66(6):1821-32. PubMed ID: 10777718
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