BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

401 related articles for article (PubMed ID: 8230157)

  • 1. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
    Burn J; Takao A; Wilson D; Cross I; Momma K; Wadey R; Scambler P; Goodship J
    J Med Genet; 1993 Oct; 30(10):822-4. PubMed ID: 8230157
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
    Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
    Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K; Kondo C; Matsuoka R
    J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.
    Takahashi K; Kido S; Hoshino K; Ogawa K; Ohashi H; Fukushima Y
    Eur J Pediatr; 1995 Nov; 154(11):878-81. PubMed ID: 8582397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.
    Matsuoka R; Kimura M; Scambler PJ; Morrow BE; Imamura S; Minoshima S; Shimizu N; Yamagishi H; Joh-o K; Watanabe S; Oyama K; Saji T; Ando M; Takao A; Momma K
    Hum Genet; 1998 Jul; 103(1):70-80. PubMed ID: 9737780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
    Momma K; Kondo C; Matsuoka R; Takao A
    Am J Cardiol; 1996 Sep; 78(5):591-4. PubMed ID: 8806353
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic basis of DiGeorge and velocardiofacial syndromes.
    Driscoll DA
    Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndrome.
    Pierpont JW; Erickson RP; Thompson FH; Yang JM
    Clin Genet; 1996 Dec; 50(6):545-7. PubMed ID: 9147896
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
    Liu AP; Chow PC; Lee PP; Mok GT; Tang WF; Lau ET; Lam ST; Chan KY; Kan AS; Chau AK; Cheung YF; Lau YL; Chung BH
    Eur J Med Genet; 2014; 57(6):306-11. PubMed ID: 24721633
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tetralogy of Fallot associated with chromosome 22q11 deletion.
    Momma K; Kondo C; Ando M; Matsuoka R; Takao A
    Am J Cardiol; 1995 Sep; 76(8):618-21. PubMed ID: 7677092
    [No Abstract]   [Full Text] [Related]  

  • 11. Anatomic patterns of conotruncal defects associated with deletion 22q11.
    Marino B; Digilio MC; Toscano A; Anaclerio S; Giannotti A; Feltri C; de Ioris MA; Angioni A; Dallapiccola B
    Genet Med; 2001; 3(1):45-8. PubMed ID: 11339377
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Frequency of 22q11 deletions in patients with conotruncal defects.
    Goldmuntz E; Clark BJ; Mitchell LE; Jawad AF; Cuneo BF; Reed L; McDonald-McGinn D; Chien P; Feuer J; Zackai EH; Emanuel BS; Driscoll DA
    J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician.
    Thomas JA; Graham JM
    Clin Pediatr (Phila); 1997 May; 36(5):253-66. PubMed ID: 9152551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA; Hatchwell E; Barber JC; Daubeney PE; Crolla JA; Salmon AP; Keeton BR; Temple IK; Dennis NR
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
    Goldmuntz E; Driscoll D; Budarf ML; Zackai EH; McDonald-McGinn DM; Biegel JA; Emanuel BS
    J Med Genet; 1993 Oct; 30(10):807-12. PubMed ID: 7901419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
    Kong CW; Cheng YKY; To WWK; Leung TY
    Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
    Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.