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Journal Abstract Search

295 related items for PubMed ID: 7747769

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov 16; 31(3):553-7. PubMed ID: 3067576
    [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 16; 33(6):507-10. PubMed ID: 8782053
    [Abstract] [Full Text] [Related]

  • 7. Proximal interstitial deletion of 7q: a case report and review of the literature.
    Zackowski JL, Raffel LJ, Blank CA, Schwartz S.
    Am J Med Genet; 1990 Jul 16; 36(3):328-32. PubMed ID: 2194394
    [Abstract] [Full Text] [Related]

  • 8. 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 16; 28(7):479-81. PubMed ID: 1895319
    [Abstract] [Full Text] [Related]

  • 9. A split hand-split foot (SHFM3) gene is located at 10q24-->25.
    Gurrieri F, Prinos P, Tackels D, Kilpatrick MW, Allanson J, Genuardi M, Vuckov A, Nanni L, Sangiorgi E, Garofalo G, Nunes ME, Neri G, Schwartz C, Tsipouras P.
    Am J Med Genet; 1996 Apr 24; 62(4):427-36. PubMed ID: 8723077
    [Abstract] [Full Text] [Related]

  • 10. Split-foot anomaly, microphthalmia, cleft-lip and cleft-palate, and mental retardation associated with a chromosome 6;13 translocation.
    Viljoen DL, Smart R.
    Clin Dysmorphol; 1993 Jul 24; 2(3):274-7. PubMed ID: 8287191
    [Abstract] [Full Text] [Related]

  • 11. 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 24; 47(2):90-5. PubMed ID: 7606850
    [Abstract] [Full Text] [Related]

  • 12. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
    Gillar PJ, Kaye CI, Ryan SG, Moore CM.
    Am J Med Genet; 1992 Sep 15; 44(2):138-41. PubMed ID: 1456281
    [Abstract] [Full Text] [Related]

  • 13. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA, Stevens MA, Byrne-Essif K, Cassidy SB.
    Am J Med Genet; 1992 Sep 01; 44(1):18-23. PubMed ID: 1519644
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 3(8):1345-54. PubMed ID: 7987313
    [Abstract] [Full Text] [Related]

  • 15. Deletion mapping of split hand/split foot malformation with hearing impairment: a case report.
    Fukushima K, Nagai K, Tsukada H, Sugata A, Sugata K, Kasai N, Kibayashi N, Maeda Y, Gunduz M, Nishizaki K.
    Int J Pediatr Otorhinolaryngol; 2003 Oct 01; 67(10):1127-32. PubMed ID: 14550969
    [Abstract] [Full Text] [Related]

  • 16. Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly.
    Correa-Cerro L, Garcíaz-Cruz D, Díaz-Castaños L, Figuera LE, Sanchez-Corona J.
    Ann Genet; 1996 Oct 01; 39(2):105-9. PubMed ID: 8766142
    [Abstract] [Full Text] [Related]

  • 17. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Oct 01; 11(1):19-24. PubMed ID: 10756423
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 15; 41(5):e54. PubMed ID: 15121782
    [No Abstract] [Full Text] [Related]

  • 20. 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]

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