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 *

651 related articles for article (PubMed ID: 123589)

  • 21. Brother and sister with trisomy 10p: a new syndrome.
    Schleiermacher E; Schliebitz U; Steffens C
    Humangenetik; 1974; 23(3):163-72. PubMed ID: 4844639
    [No Abstract]   [Full Text] [Related]  

  • 22. Trisomy 9p resulting from maternal 9/21 translocation.
    Sŭbrt I; Blehová B; Pallová B
    Hum Genet; 1976 May; 32(2):217-20. PubMed ID: 944684
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Partial trisomy 11q as the result of sporadic translocation.
    Lurie IW; Lazjuk GI; Usova YI; Gurevich DB
    Hum Genet; 1979 Sep; 51(1):63-6. PubMed ID: 500093
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial translocation t(10;21)(q22;q22).
    Delicado A; Pajares IL; Vicente P; Hawkins F
    Hum Genet; 1979 Sep; 50(3):253-8. PubMed ID: 489009
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetics of the +p9 syndrome.
    Lurie IW; Lazjuk GI; Gurevich DB; Usoev SS
    Hum Genet; 1976 Apr; 32(1):23-33. PubMed ID: 770307
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Partial trisomy 11q;22q (author's transl)].
    Benítez J; Ayuso C; García Aparicio J; Sáez E; Pérez Sotelo A; Bello MJ
    An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Partial trisomy 8 (8q24) and the trisomy-8 syndrome.
    Sánchez O; Yunis JJ
    Humangenetik; 1974; 23(4):297-303. PubMed ID: 4420964
    [No Abstract]   [Full Text] [Related]  

  • 29. Structural variation in human nitotic chromosomes.
    Leisti J
    Ann Acad Sci Fenn Biol; 1971; 179():1-69. PubMed ID: 4261167
    [No Abstract]   [Full Text] [Related]  

  • 30. Partial trisomy 7p in two families resulting from different balanced translocations.
    Moore CM; Pfeiffer RA; Craig-Holmes AP; Scott CI; Meisel-Stosiek M
    Clin Genet; 1982 Feb; 21(2):112-21. PubMed ID: 7083611
    [No Abstract]   [Full Text] [Related]  

  • 31. Segregation of two independent chromosomal translocations in one family.
    Miller K; Flatz SD
    Hum Genet; 1984; 68(1):93-5. PubMed ID: 6500562
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Complex translocation in a boy with trichorhinophalangeal syndrome.
    Sánchez LM; Labarta JD; De Negrotti TC; Migliorini AM
    J Med Genet; 1985 Aug; 22(4):314-6. PubMed ID: 4045963
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12.
    Sachdeva S; Smith GF; Justice P
    J Med Genet; 1974 Sep; 11(3):303-5. PubMed ID: 4139264
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6.
    Hustinx TW; Nabben FA; Scheres JM
    Am J Med Genet; 1979; 3(4):353-8. PubMed ID: 474635
    [No Abstract]   [Full Text] [Related]  

  • 35. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Parental origin of autosomal trisomies.
    Hassold T; Chiu D; Yamane JA
    Ann Hum Genet; 1984 May; 48(2):129-44. PubMed ID: 6234852
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Human chromosome abnormalities as related to physical and mental dysfunction.
    Heller JH
    J Hered; 1969; 60(5):239-48. PubMed ID: 4244249
    [No Abstract]   [Full Text] [Related]  

  • 38. The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred.
    Francke U; Jones KL
    Am J Dis Child; 1976 Nov; 130(11):1244-9. PubMed ID: 984008
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [On the origin of meiotic errors with special reference to trisomy 21 (author's transl)].
    Wagenbichler P
    Wien Klin Wochenschr Suppl; 1976; 63():1-23. PubMed ID: 136814
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.
    Larson LM; Wasdahl WA; Saumur JH; Coleman ML; Hall JG; Dolan CR; Schutta CJ
    Clin Genet; 1982 Mar; 21(3):187-95. PubMed ID: 7094394
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 33.