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 *

152 related articles for article (PubMed ID: 9809264)

  • 21. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
    Gerkes EH; Hordijk R; Dijkhuizen T; Sival DA; Meiners LC; Sikkema-Raddatz B; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2010; 53(5):344-6. PubMed ID: 20553986
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
    Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE
    Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Transposition of the great arteries associated with deletion of chromosome 22q11.
    Melchionda S; Digilio MC; Mingarelli R; Novelli G; Scambler P; Marino B; Dallapiccola B
    Am J Cardiol; 1995 Jan; 75(1):95-8. PubMed ID: 7801879
    [No Abstract]   [Full Text] [Related]  

  • 25. The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.
    McDonald-McGinn DM; LaRossa D; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Wang P; Solot C; Schultz P; Lynch D; Bingham P; Keenan G; Weinzimer S; Ming JE; Driscoll D; Clark BJ; Markowitz R; Cohen A; Moshang T; Pasquariello P; Randall P; Emanuel BS; Zackai EH
    Genet Test; 1997; 1(2):99-108. PubMed ID: 10464633
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Velocardiofacial syndrome presenting as hypocalcemia in early adolescence.
    Sykes KS; Bachrach LK; Siegel-Bartelt J; Ipp M; Kooh SW; Cytrynbaum C
    Arch Pediatr Adolesc Med; 1997 Jul; 151(7):745-7. PubMed ID: 9232055
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).
    Sullivan KE; McDonald-McGinn DM; Driscoll DA; Zmijewski CM; Ellabban AS; Reed L; Emanuel BS; Zackai EH; Athreya BH; Keenan G
    Arthritis Rheum; 1997 Mar; 40(3):430-6. PubMed ID: 9082929
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
    Wulfsberg EA
    Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
    [No Abstract]   [Full Text] [Related]  

  • 30. Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.
    Gothelf D; Feinstein C; Thompson T; Gu E; Penniman L; Van Stone E; Kwon H; Eliez S; Reiss AL
    Am J Psychiatry; 2007 Apr; 164(4):663-9. PubMed ID: 17403981
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Stranded, part II: Velocardiofacial syndrome, behavioral neurogenetics, and the study of developmental psychopathology.
    Feinstein C
    J Am Acad Child Adolesc Psychiatry; 2009 Nov; 48(11):1049-1050. PubMed ID: 19855217
    [No Abstract]   [Full Text] [Related]  

  • 32. Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
    Smith CA; Driscoll DA; Emanuel BS; McDonald-McGinn DM; Zackai EH; Sullivan KE
    Clin Diagn Lab Immunol; 1998 May; 5(3):415-7. PubMed ID: 9606003
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Deletion 22q11: spectrum of associated disorders.
    Hay BN
    Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Our evolving understanding of 22q.11 deletion syndrome.
    Connell F; Hodgson S
    Dev Med Child Neurol; 2005 Dec; 47(12):796. PubMed ID: 16288667
    [No Abstract]   [Full Text] [Related]  

  • 35. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.
    Gerdes M; Solot C; Wang PP; Moss E; LaRossa D; Randall P; Goldmuntz E; Clark BJ; Driscoll DA; Jawad A; Emanuel BS; McDonald-McGinn DM; Batshaw ML; Zackai EH
    Am J Med Genet; 1999 Jul; 85(2):127-33. PubMed ID: 10406665
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery].
    Pradel W; Bartsch O; Müller R; Lauer G; Eckelt U
    HNO; 2003 Sep; 51(9):755-8. PubMed ID: 12955254
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Psychosis Beyond the 22q11.2 Deletion: Do Additional Genetic Factors Play a Role?
    Goes FS; Sawa A
    Am J Psychiatry; 2017 Nov; 174(11):1027-1029. PubMed ID: 29088933
    [No Abstract]   [Full Text] [Related]  

  • 38. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).
    Perez E; Sullivan KE
    Curr Opin Pediatr; 2002 Dec; 14(6):678-83. PubMed ID: 12436034
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?
    Lévy A; Michel G; Lemerrer M; Philip N
    Am J Med Genet; 1997 Apr; 69(4):356-9. PubMed ID: 9098482
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.
    Cusmano-Ozog K; Manning MA; Hoyme HE
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):393-8. PubMed ID: 17926345
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.