BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 10546107)

  • 1. Familial deletion of 22q11.2.
    Rodríguez Criado G; Gruesomontero J; Delicado Navarro A
    Genet Couns; 1999; 10(3):325-7. PubMed ID: 10546107
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Associated anomalies in asymmetric crying facies and 22q11 deletion.
    Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M
    Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome.
    Oh AK; Workman LA; Wong GB
    Cleft Palate Craniofac J; 2007 Jan; 44(1):62-6. PubMed ID: 17214538
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
    Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [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]  

  • 7. Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission.
    Iascone MR; Vittorini S; Sacchelli M; Spadoni I; Simi P; Giusti S
    Am J Med Genet; 2002 Apr; 108(4):319-21. PubMed ID: 11920838
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Smith-Magenis syndrome and tetralogy of Fallot.
    Sweeney E; Peart I; Tofeig M; Kerr B
    J Med Genet; 1999 Jun; 36(6):501-2. PubMed ID: 10874646
    [No Abstract]   [Full Text] [Related]  

  • 9. Velocardiofacial syndrome in childhood-onset schizophrenia.
    Usiskin SI; Nicolson R; Krasnewich DM; Yan W; Lenane M; Wudarsky M; Hamburger SD; Rapoport JL
    J Am Acad Child Adolesc Psychiatry; 1999 Dec; 38(12):1536-43. PubMed ID: 10596254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
    Ford LC; Sulprizio SL; Rasgon BM
    Laryngoscope; 2000 Mar; 110(3 Pt 1):362-7. PubMed ID: 10718420
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. [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]  

  • 15. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.
    Zori RT; Boyar FZ; Williams WN; Gray BA; Bent-Williams A; Stalker HJ; Rimer LA; Nackashi JA; Driscoll DJ; Rasmussen SA; Dixon-Wood V; Williams CA
    Am J Med Genet; 1998 Apr; 77(1):8-11. PubMed ID: 9557885
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
    Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
    J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Annotation: velo-cardio-facial syndrome.
    Murphy KC
    J Child Psychol Psychiatry; 2005 Jun; 46(6):563-71. PubMed ID: 15877762
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Shprintzen (velo-cardio-facial) syndrome: a rare case.
    Alkan T; Akçevin A; Türkoglu H; Paker T; Aytaç A
    ASAIO J; 2006; 52(6):e33-4. PubMed ID: 17117043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome.
    Gothelf D; Frisch A; Munitz H; Rockah R; Laufer N; Mozes T; Hermesh H; Weizman A; Frydman M
    Schizophr Res; 1999 Jan; 35(2):105-12. PubMed ID: 9988847
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.