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 *

141 related articles for article (PubMed ID: 1877619)

  • 1. Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.
    Sharland M; Patton MA; Hill L
    Am J Med Genet; 1991 Jun; 39(4):413-4. PubMed ID: 1877619
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

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

  • 4. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C; Carvajal MV; Moscatello D; Towner J; Lacassie Y
    Am J Med Genet; 1995 Mar; 56(1):1-5. PubMed ID: 7747769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

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

  • 7. 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]  

  • 8. Monosomy 5p and trisomy 12p in a boy with familial balanced translocation.
    Vasudevan PC; Parker MJ
    Clin Dysmorphol; 2006 Apr; 15(2):85-7. PubMed ID: 16531734
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Symbrachydactyly involving hands and feet.
    De Smet L; Fabry G; Fryns JP
    Genet Couns; 1998; 9(1):23-7. PubMed ID: 9555583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ectrodactyly, cleft lip/palate syndrome.
    Rodini ES; Freitas JA; Richieri-Costa A
    Am J Med Genet; 1991 Mar; 38(4):539-41. PubMed ID: 2063894
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Counseling dilemmas in EEC syndrome.
    Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
    Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Symbrachydactyly involving hands and feet.
    Silengo M; Rabbone I; Sacchetti C
    Genet Couns; 1999; 10(2):197-8. PubMed ID: 10422017
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 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. 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]  

  • 17. 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]  

  • 18. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM
    Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.
    Boles RG; Pober BR; Gibson LH; Willis CR; McGrath J; Roberts DJ; Yang-Feng TL
    Am J Med Genet; 1995 Jan; 55(2):155-60. PubMed ID: 7717414
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entity.
    Turnpenny PD; Johnston AW; Dean JC; Haites NE; Couzin DA; Stephen GS
    Clin Dysmorphol; 1992 Apr; 1(2):103-9. PubMed ID: 1345512
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.