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 *

463 related articles for article (PubMed ID: 4085794)

  • 1. [A new case of trisomy 5p].
    Antonenko VG; Levina LIa; Chudnova VI
    Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Trisomy 5p: a report of 2 cases].
    Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A
    An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
    Menéndez I; Casaña H
    Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE; Holenova H; Braulke I
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K; Chao WT; Monaghan N; Monaco MP
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A clinical syndrome associated with dup(5p).
    Carnevale A; Hernández M; Limón-Toledo I; Frías S; Castillo J; Del Castillo V
    Am J Med Genet; 1982 Nov; 13(3):277-83. PubMed ID: 7180873
    [No Abstract]   [Full Text] [Related]  

  • 8. The 12p trisomy syndrome.
    Armendares S; Salamanca F; Nava S; Ramirez S; Cantu JM
    Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
    Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
    [TBL] [Abstract][Full Text] [Related]  

  • 10. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
    de Almeida JC; Reis DF; Llerena JC; Pereira ET
    Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
    Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
    [TBL] [Abstract][Full Text] [Related]  

  • 13. "Complete" trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p. Case report and review of the literature.
    Leschot NJ; Lim KS
    Hum Genet; 1979 Feb; 46(3):271-8. PubMed ID: 437770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B; Moore R; Mohandas T
    Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Brief clinical report: the dup(17p) syndrome.
    Feldman GM; Baumer JG; Sparkes RS
    Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.
    Clark CE; Cowell HR; Telfer MA; Casey PA
    Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 19. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F; Raoul O; Lescs MC; Danan C
    Am J Med Genet; 1985 Jul; 21(3):591-5. PubMed ID: 4025391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
    Morichon-Delvallez N; Couturier J; Frison B
    Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.