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 *

98 related articles for article (PubMed ID: 2758689)

  • 21. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
    Saad A; Khelif M; Kharrat H; Bouzakoura C
    Ann Pediatr (Paris); 1991 May; 38(5):350-4. PubMed ID: 1872531
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].
    Rethoré MO; Kaplan JC; Junien C; Cruveiller J; Dutrillaux B; Aurias A; Carpentier S; Lafourcade J; Lejeune
    Ann Genet; 1975 Jun; 18(2):81-7. PubMed ID: 1081369
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
    Duba HC; Erdel M; Löffler J; Bereuther L; Fischer H; Utermann B; Utermann G
    J Med Genet; 1997 Apr; 34(4):309-13. PubMed ID: 9138155
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndrome.
    Orye E; Craen M; Laureys G; van Coster R; van Mele B
    J Med Genet; 1985 Jun; 22(3):222-4. PubMed ID: 4009644
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A new partial trisomy 12p with artery catheter vagus, congenital cataracts, external auditory canal, and no turbinate.
    Liu YH; Xie RG; Zhang XY; Wei SD; He Y; Xu WF; Lin YY; Xiong F
    Gene; 2012 Nov; 509(1):164-7. PubMed ID: 22959136
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22.
    Parruti G; Di Ilio C; Calabrese G; Stuppia L; Guanciali Franchi P; Aceto A; Palka G
    Ann Genet; 1989; 32(1):55-8. PubMed ID: 2751250
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The 12p trisomy syndrome.
    Armendares S; Salamanca F; Nava S; Ramirez S; Cantu JM
    Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Large duplication 4q25-q34 with mild clinical effect.
    Elghezal H; Sendi HS; Monastiri K; Lapierre JM; Romdhane SI; Mougou S; Saad A
    Ann Genet; 2004; 47(4):419-22. PubMed ID: 15581841
    [TBL] [Abstract][Full Text] [Related]  

  • 29. De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells.
    Motegi T; Watanabe K; Nakamura N; Hasegawa T; Yanagawa Y
    J Med Genet; 1985 Feb; 22(1):64-6. PubMed ID: 2984424
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 31. De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberration.
    Kotzot D; Krüger C; Braun-Quentin C
    Clin Genet; 1996 Aug; 50(2):96-8. PubMed ID: 8937769
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The natural history of trisomy 12p.
    Segel R; Peter I; Demmer LA; Cowan JM; Hoffman JD; Bianchi DW
    Am J Med Genet A; 2006 Apr; 140(7):695-703. PubMed ID: 16502429
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Increase of LDH A and partial trisomy 11p (author's transl)].
    Rethoré MO; Junien C; Aurias A; Couturier J; Dutrillaux B; Kaplan JC; Lejeune J
    Ann Genet; 1980; 23(1):35-9. PubMed ID: 6965838
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines.
    Gasparini Y; Montenegro MM; Novo-Filho GM; Ceroni JRM; Honjo RS; Zanardo ÉA; Dias AT; Nascimento AM; Costa TVMM; Madia FA; Chehimi SN; Damasceno JG; Kim CA; Kulikowski LD
    Cytogenet Genome Res; 2019; 157(3):153-157. PubMed ID: 30933946
    [TBL] [Abstract][Full Text] [Related]  

  • 35. de novo inversion-duplication of 2q35-2qter without growth retardation.
    Dahoun-Hadorn S; Bretton-Chappuis B
    Ann Genet; 1992; 35(1):55-7. PubMed ID: 1610122
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
    Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
    Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 38. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
    Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
    Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: report of one case.
    Hwu WL; Kuo PL; Hung YT; Chien YH; Chu SY
    Acta Paediatr Taiwan; 2004; 45(2):97-9. PubMed ID: 15335120
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.