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 *

107 related articles for article (PubMed ID: 1746879)

  • 1. Pure 4p trisomy due to a de novo 4q;22p dicentric translocated chromosome karyotype 46,XX,-22,+t(4;22)(q1200;p13).
    de Almeida JC; Reis DF; Llerena Júnior JC
    Ann Genet; 1991; 34(2):108-10. PubMed ID: 1746879
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)].
    Stumm M; Reuter M; Mandon U; Brückner R; Wieacker P
    Klin Padiatr; 1999; 211(1):35-9. PubMed ID: 10067217
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. "Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation.
    Mikelsaar RV; Lurie IW; Ilus TE
    J Med Genet; 1996 Apr; 33(4):344-5. PubMed ID: 8730295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
    Morichon-Delvallez N; Couturier J; Frison B
    Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duplication 4q associated with chronic cholestatic changes in liver biopsy.
    Egritas O; Cavdarli B; Dalgic B; Ergun MA; Percin F; Ziegler M; Pohle B; Liehr T
    Eur J Med Genet; 2010; 53(6):411-4. PubMed ID: 20826235
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S; Mutchinick O; Shaffer LG; Fernández C
    Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocation.
    Rivas F; García-Cruz D; Rivera H; Plascencia ML; González RM; Cantú JM
    Ann Genet; 1985; 28(2):113-5. PubMed ID: 3876059
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
    Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
    Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Segregation of acrocentric chromosome association in familial dicentric Robertsonian translocation t(14p;22p), aneuploidy (trisomy-21) and heteromorphism.
    Murthy DS; Sundareshan TS; Farag TI; al-Awadi SA; al-Othman SA
    Indian J Exp Biol; 1990 Jun; 28(6):511-5. PubMed ID: 2144840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Translocation T (1;15) (Q21;P13) in a male with azoospermia].
    Antiñolo G; Borrego S; Fernández Vázquez L; Sánchez J
    Actas Urol Esp; 1989; 13(6):465-6. PubMed ID: 2618838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2;16)(p13.3;p13.3).
    Imaizumi K; Kuroki Y
    Am J Med Genet; 1991 Mar; 38(4):636-9. PubMed ID: 2063911
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
    Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identical chromosome imbalance in two siblings born to a mother with a double reciprocal translocation.
    Yardin C; Esclaire F; Gilbert B; Brosset P; Hugon J; Barthe D
    Ann Genet; 1997; 40(4):232-4. PubMed ID: 9526620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
    Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
    Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.