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 *

150 related articles for article (PubMed ID: 487639)

  • 21. 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]  

  • 22. Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations.
    Parslow M; Chambers D; Drummond M; Hunter W
    Hum Genet; 1979 Apr; 47(3):253-60. PubMed ID: 457115
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Partial trisomy 4q: two cases with a familial translocation t(4;18)(q27;q23).
    Stella M; Bonfante A; Ronconi G; Rossi G
    Hum Genet; 1979 Apr; 47(3):245-51. PubMed ID: 457114
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?
    Breuning MH; Bijlsma JB; de France HF
    Hum Genet; 1977 Aug; 38(1):7-13. PubMed ID: 903156
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial inversion translocation (8;13) with partial trisomy 13 in several family members.
    Pilgaard B; Jørgensen E; Knudsen VS; Mortensen E; Mikkelsen M
    Eur J Pediatr; 1983 Apr; 140(2):105-8. PubMed ID: 6884384
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).
    Kovacs G; Mihai C
    Hum Genet; 1979 Jun; 49(2):175-8. PubMed ID: 468247
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial trisomy 16p due to maternal balanced translocation.
    McMorrow LE; Bornstein S; Fischer RH; Gluckson MM
    J Med Genet; 1984 Aug; 21(4):315-6. PubMed ID: 6492098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Familial partial 14 trisomy.
    Miller JQ; Willson K; Wyandt H; Jaramillo MA; McConnell TS
    J Med Genet; 1979 Feb; 16(1):60-5. PubMed ID: 469889
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Trisomy 9 syndrome.
    Qazi QH; Masakawa A; Madahar C; Ehrlich R
    Clin Genet; 1977 Oct; 12(4):221-6. PubMed ID: 912938
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Characterization of partial trisomy 9p due to insertional translocation by chromosomal (micro)FISH.
    de Pater JM; Ippel PF; van Dam WM; Loneus WH; Engelen JJ
    Clin Genet; 2002 Dec; 62(6):482-7. PubMed ID: 12485198
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
    Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
    Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Abnormality of chromosome 16 and its phenotypic expression.
    Golden NL; Bilenker R; Johnson WE; Tischfield JA
    Clin Genet; 1981 Jan; 19(1):41-5. PubMed ID: 7460380
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial trisomy 12q24.31----qter.
    Tajara EH; Varella-Garcia M; Gusson AC
    J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.
    Bijlsma JB; de France HF; Bleeker-Wagemakers LM; Dijkstra PF
    Hum Genet; 1978 Jan; 40(2):135-47. PubMed ID: 624544
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Trisomy 17p due to A t(5;17) (p15;p11) pat translocation.
    Jinno Y; Matsuda I; Kajii T
    Ann Genet; 1982; 25(2):123-5. PubMed ID: 6984629
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.