BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 8023840)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.
    Crackower MA; Scherer SW; Rommens JM; Hui CC; Poorkaj P; Soder S; Cobben JM; Hudgins L; Evans JP; Tsui LC
    Hum Mol Genet; 1996 May; 5(5):571-9. PubMed ID: 8733122
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 47(6):823-31. PubMed ID: 8279479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of split hand and split foot. A case study.
    Caldwell BD
    J Am Podiatr Med Assoc; 1996 Jun; 86(6):244-8. PubMed ID: 8699344
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bilateral split hand/foot malformation and inv(7)(p22q21.3).
    Cobben JM; Verheij JB; Eisma WH; Robinson PH; Zwierstra RP; Leegte B; Castedo S
    J Med Genet; 1995 May; 32(5):375-8. PubMed ID: 7616545
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 28(7):479-81. PubMed ID: 1895319
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 140(13):1375-83. PubMed ID: 16761290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 55(4):853-5. PubMed ID: 7942863
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 33(12):996-1001. PubMed ID: 9004130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inverted insertion of chromosome 7q and ectrodactyly.
    Naritomi K; Izumikawa Y; Tohma T; Hirayama K
    Am J Med Genet; 1993 Jun; 46(5):492-3. PubMed ID: 8322806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 3(4):277-86. PubMed ID: 7894731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 122(2):191-9. PubMed ID: 17569090
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex rearrangement of chromosomes 7q21.13-q22.1 confirms the ectrodactyly-deafness locus and suggests new candidate genes.
    Bernardini L; Palka C; Ceccarini C; Capalbo A; Bottillo I; Mingarelli R; Novelli A; Dallapiccola B
    Am J Med Genet A; 2008 Jan; 146A(2):238-44. PubMed ID: 18080328
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
    Yang W; Hu ZJ; Yu XF; Li QH; Zhang AJ; Deng X; Zhang AY; Gao CS; Liu Y; Ao Y; Lo WH; Zhang X
    Zhonghua Yi Xue Za Zhi; 2006 Mar; 86(10):652-8. PubMed ID: 16681918
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.