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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

280 related items for PubMed ID: 19584065

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  • 3. 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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  • 7. 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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  • 8. Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.
    Lyle R, Radhakrishna U, Blouin JL, Gagos S, Everman DB, Gehrig C, Delozier-Blanchet C, Solanki JV, Patel UC, Nath SK, Gurrieri F, Neri G, Schwartz CE, Antonarakis SE.
    Am J Med Genet A; 2006 Jul 01; 140(13):1384-95. PubMed ID: 16691619
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  • 9. Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation.
    Dai L, Deng Y, Li N, Xie L, Mao M, Zhu J.
    BMC Med Genet; 2013 Apr 18; 14():45. PubMed ID: 23596994
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  • 10. Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization.
    Filho AB, Souza J, Faucz FR, Sotomaior VS, Dupont B, Bartel F, Rodriguez R, Schwartz CE, Skinner C, Alliman S, Raskin S.
    Am J Med Genet A; 2011 May 18; 155A(5):1152-6. PubMed ID: 21485001
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  • 11. Microduplication of BTRC detected in a Chinese family with split hand/foot malformation type 3.
    Qiu L, Li C, Zheng G, Yang T, Yang F.
    Clin Genet; 2022 Nov 18; 102(5):451-456. PubMed ID: 35908152
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  • 12. 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 18; 79(1):58-61. PubMed ID: 17120235
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  • 13. A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.
    Sidow A, Bulotsky MS, Kerrebrock AW, Birren BW, Altshuler D, Jaenisch R, Johnson KR, Lander ES.
    Nat Genet; 1999 Sep 18; 23(1):104-7. PubMed ID: 10471509
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  • 14. Split-hand/foot malformation 3 resulting from microduplications in 10q24 region in five patients from India.
    Langeh N, Ansari MT, Kabra M, Gupta N.
    Am J Med Genet A; 2024 May 18; 194(5):e63520. PubMed ID: 38168117
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  • 15. Discrepancies in upper and lower limb patterning in split hand foot malformation.
    Elliott AM, Reed MH, Roscioli T, Evans JA.
    Clin Genet; 2005 Nov 18; 68(5):408-23. PubMed ID: 16207208
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  • 17. A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.
    Ianakiev P, Kilpatrick MW, Dealy C, Kosher R, Korenberg JR, Chen XN, Tsipouras P.
    Biochem Biophys Res Commun; 1999 Jul 22; 261(1):64-70. PubMed ID: 10405324
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  • 18. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.
    Klopocki E, Lohan S, Doelken SC, Stricker S, Ockeloen CW, Soares Thiele de Aguiar R, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordass U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE, Horn D, Mundlos S.
    J Med Genet; 2012 Feb 22; 49(2):119-25. PubMed ID: 22147889
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