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 *

253 related articles for article (PubMed ID: 16470698)

  • 21. 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]  

  • 22. 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]  

  • 23. Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
    Paskulin GA; Riegel M; Cotter PD; Kiss A; Rosa RF; Zen PR; Mombach R; Graziadio C
    Am J Med Genet A; 2009 Jun; 149A(6):1302-7. PubMed ID: 19449429
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
    Gläser B; Rossier E; Barbi G; Chiaie LD; Blank C; Vogel W; Kehrer-Sawatzki H
    Am J Med Genet A; 2003 Jan; 116A(1):66-70. PubMed ID: 12476454
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter.
    Chao A; Lee YS; Chao AS; Wang TH; Chang SD
    Birth Defects Res A Clin Mol Teratol; 2006 Oct; 76(10):739-43. PubMed ID: 17022067
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.
    Dufke A; Seidel J; Schöning M; Döbler-Neumann M; Kelbova C; Liehr T; Beensen V; Backsch C; Klein-Vogler U; Enders H
    Cytogenet Cell Genet; 2000; 91(1-4):81-4. PubMed ID: 11173835
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
    Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
    Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.
    Takeno SS; Corbani M; Andrade JA; Smith Mde A; Brunoni D; Melaragno MI
    Am J Med Genet A; 2004 Aug; 129A(2):180-3. PubMed ID: 15316961
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
    Boog G; Le Vaillant C; Collet M; Dupré PF; Parent P; Bongain A; Benoit B; Trastour C
    Fetal Diagn Ther; 2004; 19(5):421-30. PubMed ID: 15305099
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.
    Nieminen P; Kotilainen J; Aalto Y; Knuutila S; Pirinen S; Thesleff I
    J Dent Res; 2003 Dec; 82(12):1013-7. PubMed ID: 14630905
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype.
    Stevenson DA; Carey JC; Cowley BC; Bayrak-Toydemir P; Mao R; Brothman AR
    J Pediatr; 2004 Dec; 145(6):840-2. PubMed ID: 15580214
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. The Wolf-Hirschhorn syndrome in fetuses.
    Tachdjian G; Fondacci C; Tapia S; Huten Y; Blot P; Nessmann C
    Clin Genet; 1992 Dec; 42(6):281-7. PubMed ID: 1493641
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.
    Okamoto N; Ohmachi K; Shimada S; Shimojima K; Yamamoto T
    Am J Med Genet A; 2013 Jun; 161A(6):1465-9. PubMed ID: 23637096
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

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