BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

360 related articles for article (PubMed ID: 12428459)

  • 1. [Phenotypic variability: genetics and chance--deletion 22q11 and schizophrenia].
    Breuning MH
    Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2016-9. PubMed ID: 12428459
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
    Lindsay EA; Greenberg F; Shaffer LG; Shapira SK; Scambler PJ; Baldini A
    Am J Med Genet; 1995 Mar; 56(2):191-7. PubMed ID: 7625444
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
    Vincent MC; Heitz F; Tricoire J; Bourrouillou G; Kuhlein E; Rolland M; Calvas P
    Genet Couns; 1999; 10(1):43-9. PubMed ID: 10191428
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
    Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
    Hjalgrim H; Hahnemann JM; Timshel S; Brøndum-Nielsen K
    Ugeskr Laeger; 2000 Jul; 162(31):4169-70. PubMed ID: 10962926
    [No Abstract]   [Full Text] [Related]  

  • 6. Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.
    Lipson A; Fagan K; Colley A; Colley P; Sholler G; Issacs D; Oates RK
    Am J Med Genet; 1996 Nov; 65(4):304-8. PubMed ID: 8923940
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Schizophrenia and the 22q11 deletion syndrome].
    Güzelcan Y; van Amelsvoort T; de Haan L; van Schaik P; Linszen DH
    Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2019-21. PubMed ID: 12428460
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Syndromes 3. Velo-cardio-facial (VCF/Shprintzen) syndrome].
    Beemer FA
    Ned Tijdschr Tandheelkd; 1998 Aug; 105(8):287-8. PubMed ID: 11928434
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA; Goldberg R; Jurecic V; Morrow B; Carlson C; Kucherlapati RS; Shprintzen RJ; Baldini A
    Am J Med Genet; 1995 Jul; 57(3):514-22. PubMed ID: 7677167
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
    Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G
    Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G; Devriendt K; Swillen A; Rommel N; Vogels A; Eyskens B; Gewillig M; Feenstra L; Fryns JP
    Genet Couns; 1999; 10(1):3-9. PubMed ID: 10191424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome).
    Digilio MC; Giannotti A; Castro M; Colistro F; Ferretti F; Marino B; Dallapiccola B
    Am J Med Genet A; 2003 Sep; 121A(3):286-8. PubMed ID: 12923874
    [No Abstract]   [Full Text] [Related]  

  • 13. [A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome].
    Vorstman JA; de Ranitz AG; Udink ten Cate FE; Beemer FA; Kahn RS
    Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2033-6. PubMed ID: 12428463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The deletions of 22q11--the Portuguese experience.
    Gaspar IM; Lourenço MT; Reis MI; Soares MA; Nogueira G; Ferreira F; Feijóo MJ
    Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Chromosome 22q11 and schizophrenia].
    Agatsuma S; Hiroi N
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2005 Apr; 25(2):79-84. PubMed ID: 16220657
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H; Ishii C; Maeda J; Kojima Y; Matsuoka R; Kimura M; Takao A; Momma K; Matsuo N
    Am J Med Genet; 1998 Jul; 78(4):319-21. PubMed ID: 9714432
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The 22q11.2 deletion syndrome.
    Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
    Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE; Howley S; Murphy KC
    Dev Disabil Res Rev; 2008; 14(1):26-34. PubMed ID: 18636634
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
    Van Esch H; Groenen P; Fryns JP; Van de Ven W; Devriendt K
    Genet Couns; 1999; 10(1):59-65. PubMed ID: 10191430
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
    Gothelf D; Schaer M; Eliez S
    Dev Disabil Res Rev; 2008; 14(1):59-68. PubMed ID: 18636637
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.