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Journal Abstract Search

82 related items for PubMed ID: 11543625

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  • 2. Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
    Shrimpton AE, Braddock BR, Thomson LL, Stein CK, Hoo JJ.
    Clin Genet; 2004 Dec; 66(6):537-44. PubMed ID: 15521982
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  • 3. Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region.
    Chaabouni M, Le Merrer M, Raoul O, Prieur M, de Blois MC, Philippe A, Vekemans M, Romana SP.
    Eur J Med Genet; 2006 Dec; 49(3):255-63. PubMed ID: 16762827
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  • 4. Chromosome mapping of the GD3 synthase gene (SIAT8) in human and mouse.
    Matsuda Y, Nara K, Watanabe Y, Saito T, Sanai Y.
    Genomics; 1996 Feb 15; 32(1):137-9. PubMed ID: 8786103
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  • 5. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).
    Shim SH, Shim JS, Min K, Lee HS, Park JE, Park SH, Hwang E, Kim M.
    Gene; 2014 Jan 15; 534(1):100-6. PubMed ID: 24095776
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  • 6. Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.
    Phelan MC, Rogers RC, Clarkson KB, Bowyer FP, Levine MA, Estabrooks LL, Severson MC, Dobyns WB.
    Am J Med Genet; 1995 Jul 31; 58(1):1-7. PubMed ID: 7573148
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  • 7. Localization of serine kinases, SRPK1 (SFRSK1) and SRPK2 (SFRSK2), specific for the SR family of splicing factors in mouse and human chromosomes.
    Wang HY, Arden KC, Bermingham JR, Viars CS, Lin W, Boyer AD, Fu XD.
    Genomics; 1999 Apr 15; 57(2):310-5. PubMed ID: 10198174
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  • 10. BID, a proapoptotic BCL-2 family member, is localized to mouse chromosome 6 and human chromosome 22q11.
    Wang K, Yin XM, Copeland NG, Gilbert DJ, Jenkins NA, Keck CL, Zimonjic DB, Popescu NC, Korsmeyer SJ.
    Genomics; 1998 Oct 15; 53(2):235-8. PubMed ID: 9790773
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  • 11. Cloning and chromosomal localization of a gene encoding a novel serine/threonine kinase belonging to the subfamily of testis-specific kinases.
    Visconti PE, Hao Z, Purdon MA, Stein P, Balsara BR, Testa JR, Herr JC, Moss SB, Kopf GS.
    Genomics; 2001 Oct 15; 77(3):163-70. PubMed ID: 11597141
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  • 15. Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.
    Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H.
    Int J Mol Med; 2004 Dec 15; 14(6):977-9. PubMed ID: 15547662
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  • 16. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
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  • 17. Chromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogene.
    Sladek R, Beatty B, Squire J, Copeland NG, Gilbert DJ, Jenkins NA, Giguère V.
    Genomics; 1997 Oct 15; 45(2):320-6. PubMed ID: 9344655
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  • 19. The mouse and human excitatory amino acid transporter gene (EAAT1) maps to mouse chromosome 15 and a region of syntenic homology on human chromosome 5.
    Kirschner MA, Arriza JL, Copeland NG, Gilbert DJ, Jenkins NA, Magenis E, Amara SG.
    Genomics; 1994 Aug 15; 22(3):631-3. PubMed ID: 8001975
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