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 *

121 related articles for article (PubMed ID: 7825599)

  • 1. Heterogeneity of the autosomal dominant split hand/split foot malformation.
    Zlotogora J
    Am J Hum Genet; 1995 Jan; 56(1):341-3. PubMed ID: 7825599
    [No Abstract]   [Full Text] [Related]  

  • 2. On the inheritance of the split hand/split foot malformation.
    Zlotogora J
    Am J Med Genet; 1994 Oct; 53(1):29-32. PubMed ID: 7802032
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Split hand/foot abnormalities: classification, pathogenesis, epidemiology].
    Elek C; Vitéz M; Czeizel E
    Orv Hetil; 1991 Jul; 132(30):1639-42. PubMed ID: 1866158
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Is there an autosomal recessive form of the split hand and split foot malformation?
    Zlotogora J; Nubani N
    J Med Genet; 1989 Feb; 26(2):138-40. PubMed ID: 2918544
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ectrodactyly and 7q22.1.
    Rivera H
    Am J Med Genet; 1994 Oct; 53(1):89-90. PubMed ID: 7802046
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M; Schapera J
    Eur J Pediatr; 1988 Feb; 147(2):202-5. PubMed ID: 3366140
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Skeletal malformations and polycystic kidney disease.
    Winter RM
    J Med Genet; 1993 Nov; 30(11):973. PubMed ID: 8301661
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Deletion mapping of split hand/split foot malformation with hearing impairment: a case report.
    Fukushima K; Nagai K; Tsukada H; Sugata A; Sugata K; Kasai N; Kibayashi N; Maeda Y; Gunduz M; Nishizaki K
    Int J Pediatr Otorhinolaryngol; 2003 Oct; 67(10):1127-32. PubMed ID: 14550969
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Brachydactyly A1: new relatives for old families?
    Girirajan S; Elsea SH
    J Genet; 2005 Aug; 84(2):95-8. PubMed ID: 16131709
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.