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 *

145 related articles for article (PubMed ID: 7239524)

  • 1. 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat.
    Stoll C; Pennerath A; Lausecker C
    Hum Genet; 1981; 56(3):413-5. PubMed ID: 7239524
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).
    Ohdo S; Madokoro H; Hayakawa K
    J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050
    [No Abstract]   [Full Text] [Related]  

  • 5. New autosomal syndromes: trisomies 4p and 9p.
    Dallapiccola B; Mastroiacovo P; Segni G
    Acta Genet Med Gemellol (Roma); 1977; 26(3-4):267-73. PubMed ID: 613692
    [No Abstract]   [Full Text] [Related]  

  • 6. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K; Howard-Peebles PN; Keele D; Friedman JM
    Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New chromosomal syndromes.
    Lewandowski RC; Yunis JJ
    Am J Dis Child; 1975 Apr; 129(4):515-29. PubMed ID: 124130
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. The phenotype of ring chromosome 3.
    Wilson GN; Pooley J; Parker J
    J Med Genet; 1982 Dec; 19(6):471-3. PubMed ID: 7154048
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).
    Kovacs G; Mihai C
    Hum Genet; 1979 Jun; 49(2):175-8. PubMed ID: 468247
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1).
    Plessis G; Couturier J; Turleau C; Despoisses S; Delavenne J
    J Med Genet; 1985 Feb; 22(1):70-3. PubMed ID: 3981584
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal recognition of 4p- syndrome.
    Blunt S; Berry AC; Seller MJ; Williams CA
    J Med Genet; 1977 Jun; 14(3):232-3. PubMed ID: 881719
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Three cases of 16q duplication.
    Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
    J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
    [No Abstract]   [Full Text] [Related]  

  • 17. De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome.
    Telvi L; Pinard JM; Ion R; Sinet PM; Nicole A; Feingold J; Dulac O; Pompidou A; Ponsot G
    J Med Genet; 1992 Oct; 29(10):747-9. PubMed ID: 1433240
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations.
    Mertens F; Johansson B; Forslund M; Olsson M; Kristoffersson U
    Clin Genet; 1987 Jul; 32(1):46-8. PubMed ID: 3621653
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Ring of the chromosome 4. I - With 4p- phenotype].
    Fraisse J; Lauras B; Couturier J; Freycon F
    Ann Genet; 1977 Jun; 20(2):101-4. PubMed ID: 302681
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Wolf-Hirschhorn syndrome. I. Genetics.
    Lurie IW; Lazjuk GI; Ussova YI; Presman EB; Gurevich DB
    Clin Genet; 1980 Jun; 17(6):375-84. PubMed ID: 7398109
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.