BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 7762585)

  • 1. Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".
    Estabrooks LL; Breg WR; Hayden MR; Ledbetter DH; Myers RM; Wyandt HE; Yang-Feng TL; Hirschhorn K
    Am J Med Genet; 1995 Feb; 55(4):453-8. PubMed ID: 7762585
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.
    Estabrooks LL; Rao KW; Driscoll DA; Crandall BF; Dean JC; Ikonen E; Korf B; Aylsworth AS
    Am J Med Genet; 1995 Jul; 57(4):581-6. PubMed ID: 7573133
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M; Murdolo M; Marangi G; Pecile V; Galasso C; Mazzanti L; Neri G
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):257-69. PubMed ID: 18932124
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
    Bi W; Cheung SW; Breman AM; Bacino CA
    Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
    Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; Memo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G
    Hum Genet; 2007 Dec; 122(5):423-30. PubMed ID: 17676343
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Identification of a critical region on chromosome 4p16.3 for Wolf-Hirschhorn syndrome-associated fetal growth retardation].
    Zheng W; Chen B; Yin Z; Huang X; Liang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):731-735. PubMed ID: 32619252
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A zinc-finger gene ZNF141 mapping at 4p16.3/D4S90 is a candidate gene for the Wolf-Hirschhorn (4p-) syndrome.
    Tommerup N; Aagaard L; Lund CL; Boel E; Baxendale S; Bates GP; Lehrach H; Vissing H
    Hum Mol Genet; 1993 Oct; 2(10):1571-5. PubMed ID: 8268908
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome.
    Altherr MR; Gusella JF; Wasmuth JJ; Kummer MA; McKercher SW; Johnson VP
    Am J Med Genet; 1992 Nov; 44(4):449-54. PubMed ID: 1442886
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion.
    Roselló M; Monfort S; Orellana C; Ferrer-Bolufer I; Quiroga R; Oltra S; Martínez F
    Cytogenet Genome Res; 2009; 125(2):103-8. PubMed ID: 19729912
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features.
    Cyr AB; Nimmakayalu M; Longmuir SQ; Patil SR; Keppler-Noreuil KM; Shchelochkov OA
    Am J Med Genet A; 2011 Sep; 155A(9):2224-8. PubMed ID: 21815251
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.
    Zollino M; Wright TJ; Di Stefano C; Tosolini A; Battaglia A; Altherr MR; Neri G
    Am J Med Genet; 1999 Feb; 82(5):371-5. PubMed ID: 10069706
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p.
    Liang D; Zhou Z; Meng D; Du J; Wen J; Niikawa N; Wu L
    Birth Defects Res A Clin Mol Teratol; 2012 Jul; 94(7):549-52. PubMed ID: 22641563
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.
    So J; Müller I; Kunath M; Herrmann S; Ullmann R; Schweiger S
    Am J Med Genet A; 2008 Jan; 146A(1):103-9. PubMed ID: 18074389
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The 4P-syndrome. Case description and literature review.
    Moretti P; Ferrari M; Di Battista S; Di Battista C
    Minerva Pediatr; 2001 Feb; 53(1):23-8. PubMed ID: 11309539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.