BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 3487279)

  • 1. Ring chromosome 11. A case report and review of the literature.
    Palka G; Verrotti A; Peca S; Mosca L; Lombardo G; Verrotti M; Morgese G
    Ann Genet; 1986; 29(1):55-8. PubMed ID: 3487279
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion of 11q: report of two cases and a review.
    Larson SA; Yeatman GW; Riccardi VM
    Birth Defects Orig Artic Ser; 1976; 12(5):125-30. PubMed ID: 953212
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
    Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV; Kapstafer KJ; Lloyd MA
    Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract]   [Full Text] [Related]  

  • 8. Ring chromosome 6: case report and review.
    Nishi Y; Yoshimura O; Ohama K; Usui T
    Am J Med Genet; 1982 May; 12(1):109-14. PubMed ID: 7091194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial 7q trisomy].
    Serville F; Broustet A; Sandler B; Bourdeau MJ; Leloup M
    Ann Genet; 1975 Mar; 18(1):67-70. PubMed ID: 1080040
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cp trisomy: a new syndrome].
    Canu JM; Buentello L; Armendares S
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA; Mikel'saar AV; Mikel'saar RV
    Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436
    [No Abstract]   [Full Text] [Related]  

  • 12. A case of ring 18 chromosome in a sibship with multiple spontaneous abortions.
    Coco R; Barreiro CZ; Penchaszadeh VB
    Ann Genet; 1975 Jun; 18(2):135-7. PubMed ID: 1081367
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The syndrome of ring chromosome 12.
    Scribanu N; McCullars EB; Baumiller RC; Colon AR
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The trisomy 9p syndrome.
    Centerwall WR; Beatty-DeSana JW
    Pediatrics; 1975 Nov; 56(5):748-55. PubMed ID: 1196731
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [Trisomy 10q24--10qter].
    Dutrillaux B; Laurent C; Bernasconi S; Lejeune J
    Ann Genet; 1975 Dec; 18(4):217-22. PubMed ID: 1083188
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The cytogenetic and clinical implications of a ring chromosome 2.
    Cote GB; Katsantoni A; Deligeorgis D
    Ann Genet; 1981; 24(4):231-5. PubMed ID: 6977305
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ring chromosome 21. Observation in a female infant.
    Carlo Stella N; Barberi I; Corrado F; Triolo O
    Ann Genet; 1984; 27(4):249-51. PubMed ID: 6335374
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.