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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

208 related items for PubMed ID: 7987314

  • 1. 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; 3(8):1355-7. PubMed ID: 7987314
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  • 2. 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; 55(1):21-6. PubMed ID: 7912888
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  • 3. 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; 3(8):1345-54. PubMed ID: 7987313
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  • 4. A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.
    Nunes ME, Schutt G, Kapur RP, Luthardt F, Kukolich M, Byers P, Evans JP.
    Hum Mol Genet; 1995 Nov; 4(11):2165-70. PubMed ID: 8589697
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  • 5. 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; 47(2):90-5. PubMed ID: 7606850
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  • 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; 33(6):507-10. PubMed ID: 8782053
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  • 7. 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; 59(1):28-36. PubMed ID: 11168022
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  • 8. 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; 55(1):12-20. PubMed ID: 8023840
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  • 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
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  • 11. Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.
    Gurrieri F, Genuardi M, Chiurazzi P, Gillessen-Kaesbach G, Neri G.
    Am J Hum Genet; 1994 Oct 24; 55(4):853-5. PubMed ID: 7942863
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  • 12. 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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  • 15. 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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  • 16. 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
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  • 18. Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature.
    Paththinige CS, Sirisena ND, Escande F, Manouvrier S, Petit F, Dissanayake VHW.
    BMC Med Genet; 2019 Jun 14; 20(1):108. PubMed ID: 31200655
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  • 19. Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.
    Naveed M, Nath SK, Gaines M, Al-Ali MT, Al-Khaja N, Hutchings D, Golla J, Deutsch S, Bottani A, Antonarakis SE, Ratnamala U, Radhakrishna U.
    Am J Hum Genet; 2007 Jan 14; 80(1):105-11. PubMed ID: 17160898
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  • 20. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.
    Babbs C, Heller R, Everman DB, Crocker M, Twigg SR, Schwartz CE, Giele H, Wilkie AO.
    Hum Genet; 2007 Sep 14; 122(2):191-9. PubMed ID: 17569090
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