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 *

158 related articles for article (PubMed ID: 8911603)

  • 1. The Wolf-Hirschhorn syndrome in adulthood: evaluation of a 24-year-old man with a rec(4) chromosome.
    Ogle R; Sillence DO; Merrick A; Ell J; Lo B; Robson L; Smith A
    Am J Med Genet; 1996 Oct; 65(2):124-7. PubMed ID: 8911603
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG; Weaver DD; Palmer CG
    Am J Med Genet; 1995 Feb; 55(4):462-5. PubMed ID: 7762587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.
    Goodship J; Curtis A; Cross I; Brown J; Emslie J; Wolstenholme J; Bhattacharya S; Burn J
    J Med Genet; 1992 Jul; 29(7):451-4. PubMed ID: 1640422
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of Wolf-Hirschhorn syndrome progressing to resistant epilepsy.
    Unalp A; Uran N; Giray O; Ercal D
    Pediatr Neurol; 2007 Aug; 37(2):140-3. PubMed ID: 17675032
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
    Fang YY; Bain S; Haan EA; Eyre HJ; MacDonald M; Wright TJ; Altherr MR; Riess O; Sutherland G; Callen DF
    Am J Med Genet; 1997 Sep; 71(4):453-7. PubMed ID: 9286454
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
    Tschernigg M; Petek E; Wagner K; Kroisel PM
    Genet Couns; 2002; 13(1):29-33. PubMed ID: 12017235
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K; Howard-Peebles PN; Keele D; Friedman JM
    Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
    Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
    Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
    Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Twenty-seven-year follow-up in the Wolf-Hirschhorn syndrome.
    Opitz JM
    Am J Med Genet; 1995 Feb; 55(4):459-61. PubMed ID: 7762586
    [No Abstract]   [Full Text] [Related]  

  • 15. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D; Krause M; Majewski F; Albrecht B; Horn D; Riess O; Gillessen-Kaesbach G
    Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.
    Ramadevi AR; Naik U; Dutta U; Srikanth ; Prabhakara K
    Am J Med Genet; 2002 Nov; 113(2):190-2. PubMed ID: 12407711
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome.
    Serville F; Saura R; Billeaud C; Girard S; Choiset A; Longy M; Sandler B
    Ann Genet; 1987; 30(3):170-4. PubMed ID: 3499855
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).
    Bocian E; Suchenek K; Obersztyn E; Nowakowska B; Mazurczak T
    J Appl Genet; 2005; 46(1):109-14. PubMed ID: 15741672
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 20. From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?
    Zollino M; Bova R; Neri G
    Am J Med Genet; 1996 Dec; 66(1):113-5. PubMed ID: 8957527
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.