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 *

183 related articles for article (PubMed ID: 739531)

  • 41. [Hypomelanosis Ito in translocation trisomy 9/mosaicism (46,XX/46,XX,t(9;9)(p24;p24)). Spontaneous remission in childhood].
    Dereser-Dennl M; Brude E; König R
    Hautarzt; 2000 Sep; 51(9):688-92. PubMed ID: 11057398
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1----p22).
    Fryns JP; Kleczkowska A; Dereymaker AM; Hoefnagels M; Heremans G; Marien J; van den Berghe H
    Clin Genet; 1985 Dec; 28(6):546-9. PubMed ID: 4075566
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Partial trisomy for the long arm of chromosome 7 due to familial balanced translocation.
    Schmid M; Wolf J; Nestler H; Krone W
    Hum Genet; 1979 Jul; 49(3):283-9. PubMed ID: 478537
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mosaicism for an additional partial chromosome 8: 46,XX/47,XX+der(8)(p21 leads to qter).
    Pfeiffer RA; Kessel E; Rathgen E; Kulenkampff M; Nehring T
    Hum Genet; 1978 Oct; 44(2):207-12. PubMed ID: 730165
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Double autosomal aberration: trisomy 21 and familial reciprocal translocation t(10;12)(p14;q21)].
    Butomo IV; Mashkova MV
    Tsitologiia; 1977 Nov; 19(11):1291-6. PubMed ID: 146289
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).
    Fryns JP; Deroover J; Haegeman J; Van den Berghe H
    Hum Genet; 1979 Mar; 47(2):217-20. PubMed ID: 437788
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Tertiary trisomy (22q11q),47,+der(22),t(11;22).
    Biederman BM; Lin CC; Lowry RB; Somerville R
    Hum Genet; 1980 Feb; 53(2):173-7. PubMed ID: 7358384
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
    Fried K; Goldberg MD; Rosenblatt M
    Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
    [No Abstract]   [Full Text] [Related]  

  • 49. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
    Fryns JP; Casaer P; Van den Berghe H
    Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. [Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization].
    Zhang J; Cai J; Yang Y; Wang S; Yao F; Huang C; Li H; Li H; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):829-832. PubMed ID: 27984615
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat.
    de Chieri P; Spatuzza E; Bonich JM
    Hum Genet; 1978 Nov; 45(1):71-5. PubMed ID: 730183
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Trisomy 4q syndrome: presentation of a new case and review of the literature.
    Lundin C; Zech L; Sjörs K; Wadelius C; Annerén G
    Ann Genet; 2002; 45(2):53-7. PubMed ID: 12119211
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
    Sills JA; Buckton KE; Raeburn JA
    J Med Genet; 1976 Dec; 13(6):507-10. PubMed ID: 1018309
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
    Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Trisomy 10p due to a de novo t(10p;13p).
    Aller V; Abrisqueta JA; Pérez-Castillo A; del Mazo J; Martín-Lucas MA; de Torres ML
    Hum Genet; 1979 Jan; 46(2):129-34. PubMed ID: 422195
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entity.
    Parloir C; Fryns JP; Van den Berghe H
    Hum Genet; 1979 Apr; 47(3):239-44. PubMed ID: 457113
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 17/7 translocation trisomy: practical vindication of a model of sickness.
    Higgs JF; Rivlin E; Taylor DC
    Arch Dis Child; 1985 Aug; 60(8):748-51. PubMed ID: 4037859
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [A mentally retarded male with multiple congenital anomalies, epilepsy and trisomy 9p and partial monosomy 17q].
    van der Linden GJ; Dumoré-Balek A; Veenema H; Geraedts JP
    Ned Tijdschr Geneeskd; 1981 Apr; 125(14):540-3. PubMed ID: 7231580
    [No Abstract]   [Full Text] [Related]  

  • 60. Interchange trisomy 9 due to maternal t(6;9) translocation.
    Ninomiya S; Narahara K; Yokoyama Y; Tsuji K; Ito S; Akahori W; Akahori T; Seino Y
    Acta Paediatr Jpn; 1994 Oct; 36(5):519-21. PubMed ID: 7825455
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.