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 *

42 related articles for article (PubMed ID: 1552546)

  • 1. Phenotypic variations in wolf-hirschhorn syndrome.
    Sukarova-Angelovska E; Kocova M; Sabolich V; Palcevska S; Angelkova N
    Balkan J Med Genet; 2014 Jun; 17(1):23-30. PubMed ID: 25741211
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.
    Wilson HL; Wong AC; Shaw SR; Tse WY; Stapleton GA; Phelan MC; Hu S; Marshall J; McDermid HE
    J Med Genet; 2003 Aug; 40(8):575-84. PubMed ID: 12920066
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome.
    Miyake N; Kurotaki N; Sugawara H; Shimokawa O; Harada N; Kondoh T; Tsukahara M; Ishikiriyama S; Sonoda T; Miyoshi Y; Sakazume S; Fukushima Y; Ohashi H; Nagai T; Kawame H; Kurosawa K; Touyama M; Shiihara T; Okamoto N; Nishimoto J; Yoshiura K; Ohta T; Kishino T; Niikawa N; Matsumoto N
    Am J Hum Genet; 2003 May; 72(5):1331-7. PubMed ID: 12687502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Toward the complete genomic map and molecular pathology of human chromosome 4.
    Riess O; Winkelmann B; Epplen JT
    Hum Genet; 1994 Jul; 94(1):1-18. PubMed ID: 8034286
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.
    McKeown C; Read AP; Dodge A; Stecko O; Mercer A; Harris R
    J Med Genet; 1987 Jul; 24(7):410-2. PubMed ID: 3612716
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. High resolution R- and G-banding on the same preparation.
    Dutrillaux B; Viegas-Pequignot E
    Hum Genet; 1981; 57(1):93-5. PubMed ID: 7262875
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.