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 *

174 related articles for article (PubMed ID: 1218860)

  • 1. Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).
    Schinzel A; Hayashi K; Schmid W
    Humangenetik; 1975 Dec; 30(4):307-16. PubMed ID: 1218860
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.
    Zaremba J; Zdzienicka E; Glogowska I; Abramowicz T; Taracha B
    J Ment Defic Res; 1974 Jun; 18(2):153-90. PubMed ID: 4141378
    [No Abstract]   [Full Text] [Related]  

  • 3. Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11).
    Binkert F; Stranzinger J; Schinzel A
    Hum Hered; 1990; 40(2):81-4. PubMed ID: 2335369
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring.
    Hansteen IL; Schirmer L; Hestetun S
    Clin Genet; 1978 Apr; 13(4):339-49. PubMed ID: 148983
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11).
    Carnevale A; Frías S; del Castillo V
    Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 10p.
    Grosse KP; Schwanitz G; Singer H; Wieczorek V
    Humangenetik; 1975 Sep; 29(2):141-4. PubMed ID: 1176136
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.
    Schinzel A
    Hum Genet; 1980 Feb; 53(2):169-72. PubMed ID: 7358383
    [TBL] [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. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.
    Schrander-Stumpel C; Schrander J; Fryns JP; Hamers G
    Clin Genet; 1990 Feb; 37(2):148-52. PubMed ID: 2178819
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.
    Orye E; Verhaaren H; Van den Bogaert-Van Heesvelde AM
    Clin Genet; 1975 Nov; 8(5):349-57. PubMed ID: 1204232
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion, del(4)(q12q21.1), owing to de novo unbalanced translocation in a 2 year old girl: further evidence that the piebald trait maps to proximal 4q12.
    Schinzel A; Braegger CP; Brecevic L; Dutly F; Binkert F
    J Med Genet; 1997 Aug; 34(8):692-5. PubMed ID: 9279767
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Orye E; Verhaaren H; Van Egmond H; Devloo-Blancquaert A
    Clin Genet; 1975 Feb; 7(2):134-43. PubMed ID: 1132161
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.
    Moedjono SJ; Sparkes RS
    Hum Genet; 1979 Sep; 50(3):241-6. PubMed ID: 489007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).
    Stoll C; Levy JM; Gardea A
    Humangenetik; 1975; 27(3):269-74. PubMed ID: 1150249
    [No Abstract]   [Full Text] [Related]  

  • 15. Ring chromosome 13 syndrome.
    Fried K; Rosenblatt M; Mundel G; Krikler R
    Clin Genet; 1975 Mar; 7(3):203-8. PubMed ID: 1139790
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy for the distal part of the long arm of chromosome 15--a new syndrome?
    Kaneko K; Katabuchi H; Maruta H
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Jun; 38(6):940-4. PubMed ID: 3734522
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 4p in a family with A t(4;15).
    Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ
    Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)].
    Woo KS; Kim KE; Kwon EY; Kim JP; Han JY
    Korean J Lab Med; 2008 Apr; 28(2):155-9. PubMed ID: 18458513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation.
    Su PH; Chen JY; Hung HM; Chen JP; Wang CM; Chen SJ
    J Formos Med Assoc; 2002 Apr; 101(4):301-3. PubMed ID: 12101870
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.