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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

265 related items for PubMed ID: 8589697

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  • 2. 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
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  • 3. Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.
    Palmer SE, Scherer SW, Kukolich M, Wijsman EM, Tsui LC, Stephens K, Evans JP.
    Am J Hum Genet; 1994 Jul 24; 55(1):21-6. PubMed ID: 7912888
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  • 4. Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.
    Raas-Rothschild A, Manouvrier S, Gonzales M, Farriaux JP, Lyonnet S, Munnich A.
    J Med Genet; 1996 Dec 24; 33(12):996-1001. PubMed ID: 9004130
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  • 5. 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 24; 3(8):1355-7. PubMed ID: 7987314
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  • 8. 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 24; 33(6):507-10. PubMed ID: 8782053
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  • 11. 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 24; 3(8):1345-54. PubMed ID: 7987313
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  • 12. 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 24; 59(1):28-36. PubMed ID: 11168022
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  • 13. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
    Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W.
    Clin Genet; 2012 Jul 24; 82(1):48-55. PubMed ID: 21554266
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  • 16. 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 24; 55(1):12-20. PubMed ID: 8023840
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