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 *

293 related articles for article (PubMed ID: 641950)

  • 1. Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).
    Niazi M; Coleman DV; Saldaña-Garcia P
    J Med Genet; 1978 Apr; 15(2):148-51. PubMed ID: 641950
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
    Rethoré MO; Lafourcade J; Couturier J; Harpey JP; Hamet M; Engler R; Alcindor LG; Lejeune J
    Ann Genet; 1982; 25(1):36-42. PubMed ID: 6979298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.
    Fried K; Bar-Yochai A; Rosenblatt M; Mundel G
    J Med Genet; 1978 Feb; 15(1):76-8. PubMed ID: 633321
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 17q. Karyotype: 46,XY,der(21),t(17;21)(q22;p13).
    Fryns JP; Parloir C; Van den Berghe H
    Hum Genet; 1979 Jul; 49(3):361-4. PubMed ID: 478542
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?
    Bass HN; Weber-Parisi F; Sparkes RS
    J Med Genet; 1978 Oct; 15(5):391-5. PubMed ID: 739531
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
    Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial trisomy 16q resulting from maternal translocation.
    Balestrazzi P; Giovannelli G; Landucci Rubini L; Dallapiccola B
    Hum Genet; 1979 Jun; 49(2):229-35. PubMed ID: 468254
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J
    J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 11q(q21 leads to qter).
    Bader PI; Jansch M; Hoffman D; Palmer CG; Gerber H; Taylor G
    Birth Defects Orig Artic Ser; 1978; 14(6C):383-92. PubMed ID: 728594
    [No Abstract]   [Full Text] [Related]  

  • 11. Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.
    Nakai H; Yamamoto Y; Kuroki Y
    Hum Genet; 1979 Oct; 51(3):349-55. PubMed ID: 511169
    [No Abstract]   [Full Text] [Related]  

  • 12. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.
    Assawamakin A; Wattanasirichaigoon D; Tocharoentanaphol C; Waeteekul S; Tansatit M; Thongnoppakhun W; Limwongse C
    Am J Med Genet A; 2012 Apr; 158A(4):901-8. PubMed ID: 22419381
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of partial trisomy 17 resulting from X-autosomal translocation.
    Yamamoto Y; Endo Y; Kuroki Y
    J Med Genet; 1979 Oct; 16(5):395-9. PubMed ID: 513087
    [TBL] [Abstract][Full Text] [Related]  

  • 16. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5).
    Gilgenkrantz S; Dulucq P; Bresson JL; Gouget A; Pernot C; Gregoire MJ
    J Med Genet; 1981 Dec; 18(6):465-9. PubMed ID: 7334508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy 3p syndrome.
    Reiss JA; Sheffield LJ; Sutherland GR
    Clin Genet; 1986 Jul; 30(1):50-8. PubMed ID: 3757296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.
    Roberts SH; Duckett DP
    J Med Genet; 1978 Oct; 15(5):375-81. PubMed ID: 739528
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333).
    Beemer FA; de France HF; Rosina-Angelista IJ; Gerards LJ; Cats BP; Guyt R
    Clin Genet; 1984 Sep; 26(3):209-15. PubMed ID: 6478641
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.