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 *

120 related articles for article (PubMed ID: 3233781)

  • 1. A photometer used for diagnosing a small-sized 4p deletion in Wolf syndrome.
    Léonard C; Huret JL
    Clin Genet; 1988 Oct; 34(4):276-8. PubMed ID: 3233781
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
    Gonzalez CH; Capelozzi VL; Wajntal A
    Am J Med Genet; 1981; 9(3):183-7. PubMed ID: 7282779
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease.
    Ikonen E; Salo A; Somer M; Somer H; Pääkkönen L; Peltonen L
    Am J Med Genet; 1992 Jul; 43(4):753-8. PubMed ID: 1535752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.
    Martsolf JT; Chase TR; Jalal SM; Wasdahl WA
    Clin Genet; 1987 Jun; 31(6):366-9. PubMed ID: 3621637
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wolf-Hirschhorn(4p-) syndrome.
    Mathai S; Ganguly BB
    Indian Pediatr; 2003 Jul; 40(7):681. PubMed ID: 12881629
    [No Abstract]   [Full Text] [Related]  

  • 8. Wolf-Hirschhorn (4p deletion) syndrome: report of one case.
    Tan CK; Tsai FJ; Lin CC; Wu JY; Yu MT; Hsu SL; Shi YR; Chang JC; Lai SW
    Acta Paediatr Taiwan; 2000; 41(1):39-42. PubMed ID: 10910559
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
    Fryns JP; Smeets E; Devriendt K; Petit P
    Ann Genet; 1998; 41(2):73-6. PubMed ID: 9706336
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interstitial deletion of 4(q21q25) in a liveborn male.
    Rose NC; Schneider A; McDonald-McGinn DM; Caserta C; Emanuel BS; Zackai EH
    Am J Med Genet; 1991 Jul; 40(1):77-9. PubMed ID: 1887853
    [TBL] [Abstract][Full Text] [Related]  

  • 11. De novo 4p-syndrome with oligohydramnios sequence.
    Su PH; Kuo PL; Chen SJ; Hung HM; Yi TH; Chen JY
    J Formos Med Assoc; 2003 Sep; 102(9):647-9. PubMed ID: 14625611
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype.
    Manouvrier S; Boute O; Viot G; Delobel B
    Clin Genet; 1999 Feb; 55(2):127-9. PubMed ID: 10189091
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p.
    Seiberth V; Kachel W; Knorz MC; Liesenhoff H
    Am J Ophthalmol; 1994 Mar; 117(3):411-3. PubMed ID: 8129026
    [No Abstract]   [Full Text] [Related]  

  • 15. Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).
    Wieczorek D; Krause M; Majewski F; Albrecht B; Meinecke P; Riess O; Gillessen-Kaesbach G
    J Med Genet; 2000 Oct; 37(10):798-804. PubMed ID: 11183188
    [No Abstract]   [Full Text] [Related]  

  • 16. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP; Yang-Aisheng ; Kleczkowska A; Lemmens F; Vandecasseye W; van den Berghe H
    Ann Genet; 1989; 32(1):59-61. PubMed ID: 2751251
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Rieger syndrome and interstitial 4q26 deletion.
    Fryns JP; Van Den Berghe H
    Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
    [No 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. 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]  

    [Next]    [New Search]
    of 6.