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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 1877619

  • 1. 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]

  • 2. 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]

  • 3. Ectrodactyly and 7q22.1.
    Rivera H.
    Am J Med Genet; 1994 Oct 15; 53(1):89-90. PubMed ID: 7802046
    [No Abstract] [Full Text] [Related]

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  • 5. 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 15; 32(5):375-8. PubMed ID: 7616545
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 15; 3(4):277-86. PubMed ID: 7894731
    [Abstract] [Full Text] [Related]

  • 8. Monosomy 5p and trisomy 12p in a boy with familial balanced translocation.
    Vasudevan PC, Parker MJ.
    Clin Dysmorphol; 2006 Apr 15; 15(2):85-7. PubMed ID: 16531734
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  • 10. Ectrodactyly, cleft lip/palate syndrome.
    Rodini ES, Freitas JA, Richieri-Costa A.
    Am J Med Genet; 1991 Mar 15; 38(4):539-41. PubMed ID: 2063894
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Jan 15; 11(1):19-24. PubMed ID: 10756423
    [Abstract] [Full Text] [Related]

  • 13. Symbrachydactyly involving hands and feet.
    Silengo M, Rabbone I, Sacchetti C.
    Genet Couns; 1999 Jan 15; 10(2):197-8. PubMed ID: 10422017
    [No Abstract] [Full Text] [Related]

  • 14. Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.
    Roberts SH, Hughes HE, Davies SJ, Meredith AL.
    J Med Genet; 1991 Jul 15; 28(7):479-81. PubMed ID: 1895319
    [Abstract] [Full Text] [Related]

  • 15. Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.
    Genuardi M, Pomponi MG, Sammito V, Bellussi A, Zollino M, Neri G.
    Am J Med Genet; 1993 Nov 01; 47(6):823-31. PubMed ID: 8279479
    [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 01; 47(2):90-5. PubMed ID: 7606850
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 3(8):1355-7. PubMed ID: 7987314
    [Abstract] [Full Text] [Related]

  • 18. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Aug 01; 13(3):303-7. PubMed ID: 12416638
    [Abstract] [Full Text] [Related]

  • 19. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG, Pober BR, Gibson LH, Willis CR, McGrath J, Roberts DJ, Yang-Feng TL.
    Am J Med Genet; 1995 Jan 16; 55(2):155-60. PubMed ID: 7717414
    [Abstract] [Full Text] [Related]

  • 20. Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entity.
    Turnpenny PD, Johnston AW, Dean JC, Haites NE, Couzin DA, Stephen GS.
    Clin Dysmorphol; 1992 Apr 16; 1(2):103-9. PubMed ID: 1345512
    [Abstract] [Full Text] [Related]

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