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 *

162 related articles for article (PubMed ID: 1424245)

  • 1. Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.
    Thies U; Back E; Wolff G; Schroeder-Kurth T; Hager HD; Schröder K
    Clin Genet; 1992 Oct; 42(4):201-5. PubMed ID: 1424245
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
    Estabrooks LL; Lamb AN; Aylsworth AS; Callanan NP; Rao KW
    J Med Genet; 1994 Feb; 31(2):103-7. PubMed ID: 8182713
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
    Estabrooks LL; Rao KW; Korf B
    Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.
    Anvret M; Nordenskjöld M; Stolpe L; Johansson L; Bröndum-Nielsen K
    Hum Genet; 1991 Mar; 86(5):481-3. PubMed ID: 2016087
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
    Finzi S; Pinto CF; Wiggs JL
    Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].
    Wilson MG; Towner JW; Coffin GS; Ebbin AJ; Siris E; Brager P
    Hum Genet; 1981; 59(4):297-307. PubMed ID: 6949855
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
    South ST; Whitby H; Maxwell T; Aston E; Brothman AR; Carey JC
    Am J Med Genet A; 2008 Oct; 146A(20):2691-7. PubMed ID: 18798325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.
    Altherr MR; Wright TJ; Denison K; Perez-Castro AV; Johnson VP
    Am J Med Genet; 1997 Jul; 71(1):47-53. PubMed ID: 9215768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.
    Quarrell OW; Snell RG; Curtis MA; Roberts SH; Harper PS; Shaw DJ
    J Med Genet; 1991 Apr; 28(4):256-9. PubMed ID: 1856831
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.
    Zollino M; Di Stefano C; Zampino G; Mastroiacovo P; Wright TJ; Sorge G; Selicorni A; Tenconi R; Zappalà A; Battaglia A; Di Rocco M; Palka G; Pallotta R; Altherr MR; Neri G
    Am J Med Genet; 2000 Sep; 94(3):254-61. PubMed ID: 10995514
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.
    Kant SG; Van Haeringen A; Bakker E; Stec I; Donnai D; Mollevanger P; Beverstock GC; Lindeman-Kusse MC; Van Ommen GJ
    J Med Genet; 1997 Jul; 34(7):569-72. PubMed ID: 9222965
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat.
    el-Rifai W; Leisti J; Kähkönen M; Pietarinen A; Altherr MR; Knuutila S
    J Med Genet; 1995 Jan; 32(1):65-7. PubMed ID: 7897631
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
    Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.
    Zollino M; Lecce R; Selicorni A; Murdolo M; Mancuso I; Marangi G; Zampino G; Garavelli L; Ferrarini A; Rocchi M; Opitz JM; Neri G
    Eur J Hum Genet; 2004 Oct; 12(10):797-804. PubMed ID: 15241479
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome.
    Gandelman KY; Gibson L; Meyn MS; Yang-Feng TL
    Am J Hum Genet; 1992 Sep; 51(3):571-8. PubMed ID: 1379774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis redefines three human chromosome 14 deletions.
    Wintle RF; Costa T; Haslam RH; Teshima IE; Cox DW
    Hum Genet; 1995 May; 95(5):495-500. PubMed ID: 7759068
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.
    Tupler R; Bortotto L; Bühler EM; Alkan M; Malik NJ; Bösch-Al Jadooa N; Memo L; Maraschio P
    J Med Genet; 1992 Jan; 29(1):53-5. PubMed ID: 1552546
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome.
    Dallapiccola B; Mandich P; Bellone E; Selicorni A; Mokin V; Ajmar F; Novelli G
    Am J Med Genet; 1993 Nov; 47(6):921-4. PubMed ID: 7904122
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial interstitial deletion of the short arm of chromosome 4 (p15.33-p16.3) characterized by molecular cytogenetic analysis.
    Basinko A; Douet-Guilbert N; Parent P; Blondin G; Mingam M; Monot F; Morel F; Le Bris MJ; De Braekeleer M
    Am J Med Genet A; 2008 Apr; 146A(7):899-903. PubMed ID: 18302281
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.