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 *

295 related articles for article (PubMed ID: 7490915)

  • 1. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.
    Crifasi PA; Michels VV; Driscoll DJ; Jalal SM; Dewald GW
    Mayo Clin Proc; 1995 Dec; 70(12):1148-53. PubMed ID: 7490915
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. CATCH 22 Syndrome.
    Yonehara Y; Nakatsuka T; Ichioka S; Sasaki N; Kobayashi T
    J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Microdeletion 22q11 in complex cardiovascular malformations.
    Mehraein Y; Wippermann CF; Michel-Behnke I; Nhan Ngo TK; Hillig U; Giersberg M; Aulepp U; Barth H; Fritz B; Rehder H
    Hum Genet; 1997 Apr; 99(4):433-42. PubMed ID: 9099830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.
    Scambler PJ; Kelly D; Lindsay E; Williamson R; Goldberg R; Shprintzen R; Wilson DI; Goodship JA; Cross IE; Burn J
    Lancet; 1992 May; 339(8802):1138-9. PubMed ID: 1349369
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
    Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS
    J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2.
    Li M; Zackai EH; Niikawa N; Kaplan P; Driscoll DA
    Am J Med Genet; 1996 Oct; 65(2):101-3. PubMed ID: 8911598
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Psychiatric inpatients and chromosome deletions within 22q11.2.
    Sugama S; Namihira T; Matsuoka R; Taira N; Eto Y; Maekawa K
    J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):803-6. PubMed ID: 10567504
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
    McDonald-McGinn DM; Driscoll DA; Emanuel BS; Goldmuntz E; Clark BJ; Solot C; Cohen M; Schultz P; LaRossa D; Randall P; Zackai EH
    Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.
    Cuneo BF
    Curr Opin Pediatr; 2001 Oct; 13(5):465-72. PubMed ID: 11801894
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.