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Journal Abstract Search

214 related items for PubMed ID: 11754066

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  • 3. Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.
    Ogata T, Wakui K, Kosho T, Muroya K, Yamanouchi Y, Takano T, Fukushima Y, Rappold G, Suzuki Y.
    Am J Med Genet; 2000 Jun 05; 92(4):256-9. PubMed ID: 10842291
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  • 5. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.
    Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, Eash D, Ledbetter DH, Martin CL.
    J Med Genet; 2006 Jun 05; 43(6):478-89. PubMed ID: 16199540
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  • 7. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
    Marozzi A, Manfredini E, Tibiletti MG, Furlan D, Villa N, Vegetti W, Crosignani PG, Ginelli E, Meneveri R, Dalprà L.
    Hum Genet; 2000 Oct 05; 107(4):304-11. PubMed ID: 11129329
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  • 8. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome.
    Wydner KL, Li M, Singer-Granick C, Sciorra LJ, Krueger LJ.
    Am J Med Genet; 1995 Mar 27; 56(2):141-6. PubMed ID: 7625435
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  • 10. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.
    Chin Med J (Engl); 2003 Sep 27; 116(9):1298-303. PubMed ID: 14527352
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  • 11. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J, van Haeringen A, Hansson KB, Lankester A, Smit MJ, Belfroid RD, Bakker E, Rosenberg C, Tanke HJ, Szuhai K.
    Eur J Hum Genet; 2007 May 27; 15(5):548-55. PubMed ID: 17342151
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  • 12. Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.
    Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N.
    J Clin Endocrinol Metab; 2000 Aug 27; 85(8):2927-30. PubMed ID: 10946905
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  • 15. The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.
    Therman E, Susman B.
    Hum Genet; 1990 Jul 27; 85(2):175-83. PubMed ID: 2370045
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  • 17. Short stature in a mother and daughter with terminal deletion of Xp22.3.
    Schwinger E, Kirschstein M, Greiwe M, Konermann T, Orth U, Gal A.
    Am J Med Genet; 1996 May 03; 63(1):239-42. PubMed ID: 8723116
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