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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for PubMed ID: 18080328

  • 1. Complex rearrangement of chromosomes 7q21.13-q22.1 confirms the ectrodactyly-deafness locus and suggests new candidate genes.
    Bernardini L, Palka C, Ceccarini C, Capalbo A, Bottillo I, Mingarelli R, Novelli A, Dallapiccola B.
    Am J Med Genet A; 2008 Jan 15; 146A(2):238-44. PubMed ID: 18080328
    [Abstract] [Full Text] [Related]

  • 2. Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.
    Ignatius J, Knuutila S, Scherer SW, Trask B, Kere J.
    J Med Genet; 1996 Jun 15; 33(6):507-10. PubMed ID: 8782053
    [Abstract] [Full Text] [Related]

  • 3. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
    [Abstract] [Full Text] [Related]

  • 4. Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.
    Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui LC.
    Hum Mol Genet; 1996 May 13; 5(5):571-9. PubMed ID: 8733122
    [Abstract] [Full Text] [Related]

  • 5. Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly.
    Scherer SW, Poorkaj P, Massa H, Soder S, Allen T, Nunes M, Geshuri D, Wong E, Belloni E, Little S.
    Hum Mol Genet; 1994 Aug 13; 3(8):1345-54. PubMed ID: 7987313
    [Abstract] [Full Text] [Related]

  • 6. Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.
    Wieland I, Muschke P, Jakubiczka S, Volleth M, Freigang B, Wieacker PF.
    J Med Genet; 2004 May 13; 41(5):e54. PubMed ID: 15121782
    [No Abstract] [Full Text] [Related]

  • 7. Bilateral split hand/foot malformation and inv(7)(p22q21.3).
    Cobben JM, Verheij JB, Eisma WH, Robinson PH, Zwierstra RP, Leegte B, Castedo S.
    J Med Genet; 1995 May 13; 32(5):375-8. PubMed ID: 7616545
    [Abstract] [Full Text] [Related]

  • 8. A contiguous gene deletion syndrome at 7q21-q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly.
    Nunes ME, Pagon RA, Disteche CJ, Evans JP.
    Clin Dysmorphol; 1994 Oct 13; 3(4):277-86. PubMed ID: 7894731
    [Abstract] [Full Text] [Related]

  • 9. Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.
    Sharland M, Patton MA, Hill L.
    Am J Med Genet; 1991 Jun 15; 39(4):413-4. PubMed ID: 1877619
    [Abstract] [Full Text] [Related]

  • 10. Characterization of the complex 7q21.3 rearrangement in a patient with bilateral split-foot malformation and hearing loss.
    Saitsu H, Kurosawa K, Kawara H, Eguchi M, Mizuguchi T, Harada N, Kaname T, Kano H, Miyake N, Toda T, Matsumoto N.
    Am J Med Genet A; 2009 Jun 15; 149A(6):1224-30. PubMed ID: 19449426
    [Abstract] [Full Text] [Related]

  • 11. Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.
    Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S, Stephens K, Pagon RA, Patton MA.
    Am J Hum Genet; 1994 Jul 15; 55(1):12-20. PubMed ID: 8023840
    [Abstract] [Full Text] [Related]

  • 12. Inverted insertion of chromosome 7q and ectrodactyly.
    Naritomi K, Izumikawa Y, Tohma T, Hirayama K.
    Am J Med Genet; 1993 Jun 15; 46(5):492-3. PubMed ID: 8322806
    [Abstract] [Full Text] [Related]

  • 13. The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.
    Slavotinek A, Maher E, Gregory P, Rowlandson P, Huson SM.
    J Med Genet; 1997 Oct 15; 34(10):857-61. PubMed ID: 9350823
    [Abstract] [Full Text] [Related]

  • 14. Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH.
    Tzschach A, Menzel C, Erdogan F, Schubert M, Hoeltzenbein M, Barbi G, Petzenhauser C, Ropers HH, Ullmann R, Kalscheuer V.
    Am J Med Genet A; 2007 Feb 15; 143(4):333-7. PubMed ID: 17230488
    [Abstract] [Full Text] [Related]

  • 15. Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2.
    David D, Marques B, Ferreira C, Vieira P, Corona-Rivera A, Ferreira JC, van Bokhoven H.
    Eur J Hum Genet; 2009 Aug 15; 17(8):1024-33. PubMed ID: 19223936
    [Abstract] [Full Text] [Related]

  • 16. Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1.
    Marinoni JC, Stevenson RE, Evans JP, Geshuri D, Phelan MC, Schwartz CE.
    Clin Genet; 1995 Feb 15; 47(2):90-5. PubMed ID: 7606850
    [Abstract] [Full Text] [Related]

  • 17. Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.
    Tackels-Horne D, Toburen A, Sangiorgi E, Gurrieri F, de Mollerat X, Fischetto R, Causio F, Clarkson K, Stevenson RE, Schwartz CE.
    Clin Genet; 2001 Jan 15; 59(1):28-36. PubMed ID: 11168022
    [Abstract] [Full Text] [Related]

  • 18. Genetics of split hand and split foot. A case study.
    Caldwell BD.
    J Am Podiatr Med Assoc; 1996 Jun 15; 86(6):244-8. PubMed ID: 8699344
    [Abstract] [Full Text] [Related]

  • 19. Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.
    Marinoni JC, Boyd E, Sherman S, Schwartz C.
    Hum Mol Genet; 1994 Aug 15; 3(8):1355-7. PubMed ID: 7987314
    [Abstract] [Full Text] [Related]

  • 20. An interstitial deletion of chromosome 7 at band q21: a case report and review.
    Courtens W, Vermeulen S, Wuyts W, Messiaen L, Wauters J, Nuytinck L, Peeters N, Storm K, Speleman F, Nöthen MM.
    Am J Med Genet A; 2005 Apr 01; 134A(1):12-23. PubMed ID: 15732063
    [Abstract] [Full Text] [Related]

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