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 *

256 related articles for article (PubMed ID: 17569090)

  • 41. Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
    Kano H; Kurosawa K; Horii E; Ikegawa S; Yoshikawa H; Kurahashi H; Toda T
    Hum Genet; 2005 Dec; 118(3-4):477-83. PubMed ID: 16235095
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Split hand foot malformation (SHFM).
    Elliott AM; Evans JA; Chudley AE
    Clin Genet; 2005 Dec; 68(6):501-5. PubMed ID: 16283879
    [TBL] [Abstract][Full Text] [Related]  

  • 43. New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene.
    Crippa M; Bestetti I; Perotti M; Castronovo C; Tabano S; Picinelli C; Grassi G; Larizza L; Pincelli AI; Finelli P
    BMC Med Genet; 2014 May; 15():52. PubMed ID: 24886451
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly.
    Lodder EM; Eussen BH; van Hassel DA; Hoogeboom AJ; Poddighe PJ; Coert JH; Oostra BA; de Klein A; de Graaff E
    Chromosome Res; 2009; 17(6):737-44. PubMed ID: 19672683
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A; de Miranda E; Kamiya TY; Freire-Maia DV
    Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective.
    Klar AJ
    Dev Biol; 2015 Dec; 408(1):7-13. PubMed ID: 26477560
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation.
    Ugur SA; Tolun A
    Hum Mol Genet; 2008 Sep; 17(17):2644-53. PubMed ID: 18515319
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. [Genetic analysis of three families affected with split-hand/split-foot malformation].
    He W; Lin G; Liang P; Cheng D; Hu X; Zhou L; Xiong B; Tan Y; Lu G; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):476-480. PubMed ID: 28777841
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Discrepancies in upper and lower limb patterning in split hand foot malformation.
    Elliott AM; Reed MH; Roscioli T; Evans JA
    Clin Genet; 2005 Nov; 68(5):408-23. PubMed ID: 16207208
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.
    Wieland I; Muschke P; Jakubiczka S; Volleth M; Freigang B; Wieacker PF
    J Med Genet; 2004 May; 41(5):e54. PubMed ID: 15121782
    [No Abstract]   [Full Text] [Related]  

  • 55. Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.
    Ianakiev P; Kilpatrick MW; Toudjarska I; Basel D; Beighton P; Tsipouras P
    Am J Hum Genet; 2000 Jul; 67(1):59-66. PubMed ID: 10839977
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. The expanding panorama of split hand foot malformation.
    Basel D; Kilpatrick MW; Tsipouras P
    Am J Med Genet A; 2006 Jul; 140(13):1359-65. PubMed ID: 16763964
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance.
    Blattner A; Huber AR; Röthlisberger B
    Am J Med Genet A; 2010 Aug; 152A(8):2053-6. PubMed ID: 20635353
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 13.