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 *

133 related articles for article (PubMed ID: 477015)

  • 21. [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]  

  • 22. Familial partial trisomy 6q syndromes resulting from inherited ins (5;6) (q33;q15q27).
    Chen H; Tyrkus M; Cohen F; Woolley PV; Mayeda K; Bhogaonker A; Espirtu CE; Simpson W
    Clin Genet; 1976 Jun; 9(6):631-7. PubMed ID: 1277576
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
    Stengel-Rutkowski S; Warkotsch A; Schimanek P; Stene J
    Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
    [TBL] [Abstract][Full Text] [Related]  

  • 25. "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]  

  • 26. 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]  

  • 27. Multiple congenital defects associated with trisomy for long arm of No. 4.
    Issa M; Potter AM; Blank CE
    J Med Genet; 1976 Aug; 13(4):326-9. PubMed ID: 957383
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial duplication of distal 17q.
    Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
    Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS; Lewis FJ; Vowles M
    J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. [Partial 4q trisomy. Apropos of 3 cases].
    Dutrillaux B; Laurent C; Forabosco A; Noel B; Suerinc E; Biemont MC; Cotton JB
    Ann Genet; 1975 Mar; 18(1):21-7. PubMed ID: 238457
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
    Tranebjaerg L; Baekmark UB; Dyhr-Nielsen M; Kreiborg S
    Clin Genet; 1987 Aug; 32(2):137-43. PubMed ID: 3652493
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.
    Schinzel A; Schmid W; Auf der Maur P; Moser H; Degenhardt KH; Geisler M; Grubisic A
    Hum Genet; 1981; 56(3):249-62. PubMed ID: 7239508
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Partial distal trisomy 13q resulting from familial reciprocal 5/13 translocation.
    Yanagisawa S; Yokoyama H; Agena N
    Hum Genet; 1978 Dec; 45(3):345-50. PubMed ID: 738734
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.
    Gouw WL; Anders GJ; ten Kate LP; de Groot CJ
    Humangenetik; 1972; 16(3):251-9. PubMed ID: 5082106
    [No Abstract]   [Full Text] [Related]  

  • 36. Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndrome.
    Salazar D; Rosenfeld W; Verma RS; Jhaveri RC; Dosik H
    Am J Dis Child; 1979 Oct; 133(10):1006-8. PubMed ID: 495588
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
    Kessel E; Pfeiffer RA; Kosenow W
    Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.