These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 8589697)

  • 1. 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]  

  • 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; 62(4):427-36. PubMed ID: 8723077
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 55(1):21-6. PubMed ID: 7912888
    [TBL] [Abstract][Full Text] [Related]  

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

  • 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; 3(8):1355-7. PubMed ID: 7987314
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.
    Ozen RS; Baysal BE; Devlin B; Farr JE; Gorry M; Ehrlich GD; Richard CW
    Am J Hum Genet; 1999 Jun; 64(6):1646-54. PubMed ID: 10330351
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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; 33(6):507-10. PubMed ID: 8782053
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetic characterization of a Korean split hand/split foot malformation (SHFM).
    Kang YS; Cheong HM; Moon Y; Lee IB; Kim SM; Kim HS; Jun SY; Jung SK; Kim JS; Choi JH; Cho HE; Son JS; Min NY; Lee KH
    Mol Cells; 2004 Jun; 17(3):397-403. PubMed ID: 15232212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 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; 3(8):1345-54. PubMed ID: 7987313
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 59(1):28-36. PubMed ID: 11168022
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 82(1):48-55. PubMed ID: 21554266
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Wolf-Hirschhorn syndrome and a split-hand malformation.
    Bamshad M; O'Quinn JR; Carey JC
    Am J Med Genet; 1998 Feb; 75(4):351-4. PubMed ID: 9482640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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; 55(1):12-20. PubMed ID: 8023840
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 140(13):1384-95. PubMed ID: 16691619
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 21(6):357-362. PubMed ID: 28422522
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.
    Faiyaz ul Haque M; Uhlhaas S; Knapp M; Schüler H; Friedl W; Ahmad M; Propping P
    Hum Genet; 1993 Mar; 91(1):17-9. PubMed ID: 8454282
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 124A(2):136-41. PubMed ID: 14699611
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.