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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for PubMed ID: 14699611

  • 1. The 10q24-linked split hand/split foot syndrome (SHFM3): narrowing of the critical region and confirmation of the clinical phenotype.
    Roscioli T, Taylor PJ, Bohlken A, Donald JA, Masel J, Glass IA, Buckley MF.
    Am J Med Genet A; 2004 Jan 15; 124A(2):136-41. PubMed ID: 14699611
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  • 4. Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
    Everman DB, Morgan CT, Lyle R, Laughridge ME, Bamshad MJ, Clarkson KB, Colby R, Gurrieri F, Innes AM, Roberson J, Schrander-Stumpel C, van Bokhoven H, Antonarakis SE, Schwartz CE.
    Am J Med Genet A; 2006 Jul 01; 140(13):1375-83. PubMed ID: 16761290
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  • 10. Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3.
    Gurnett CA, Dobbs MB, Nordsieck EJ, Keppel C, Goldfarb CA, Morcuende JA, Bowcock AM.
    Am J Med Genet A; 2006 Aug 15; 140(16):1744-8. PubMed ID: 16838310
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  • 11. 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 15; 82(1):48-55. PubMed ID: 21554266
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  • 13. Triphalangeal thumb in association with split hand/foot: a phenotypic marker for SHFM3?
    Elliott AM, Reed MH, Evans JA.
    Birth Defects Res A Clin Mol Teratol; 2007 Jan 15; 79(1):58-61. PubMed ID: 17120235
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  • 14. Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.
    Elliott AM, Evans JA.
    Am J Med Genet A; 2006 Jul 01; 140(13):1419-27. PubMed ID: 16688749
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  • 15. Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
    Dimitrov BI, de Ravel T, Van Driessche J, de Die-Smulders C, Toutain A, Vermeesch JR, Fryns JP, Devriendt K, Debeer P.
    J Med Genet; 2010 Feb 01; 47(2):103-11. PubMed ID: 19584065
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  • 16. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
    Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE.
    Am J Med Genet; 1999 Jul 30; 85(3):236-42. PubMed ID: 10398235
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  • 17. Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.
    Cao L, Yang W, Wang S, Chen C, Zhang X, Luo Y.
    Genet Test Mol Biomarkers; 2017 Jun 30; 21(6):357-362. PubMed ID: 28422522
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  • 18. [Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis].
    Zhang XQ, Wang J, Xiong F, Lv WB, Zhou YQ, Yang SM, Zhang YT, Tian XY, Lian W, Xu XM.
    Yi Chuan; 2019 Aug 20; 41(8):716-724. PubMed ID: 31447422
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  • 20. 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 20; 3(8):1355-7. PubMed ID: 7987314
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