BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

686 related articles for article (PubMed ID: 11464533)

  • 21. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
    Shuib S; Abdul Latif Z; Abidin NZ; Akmal SN; Zakaria Z
    Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857
    [TBL] [Abstract][Full Text] [Related]  

  • 22. DiGeorge syndrome: new insights.
    Goldmuntz E
    Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Concurrent microdeletion and duplication of 22q11.2.
    Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
    Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.
    Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Chromosome 22q11 deletion syndrome: the first three cases reported in Thailand.
    Ruangdaraganon N; Tocharoentanaphol C; Khowsathit P; Sombuntham T; Pongpanich B
    J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S179-85. PubMed ID: 10730540
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
    Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Prenatal diagnosis of 22q11 microdeletion.
    Levy-Mozziconacci A; Piquet C; Heurtevin PC; Philip N
    Prenat Diagn; 1997 Nov; 17(11):1033-7. PubMed ID: 9399351
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
    Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV
    Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [DiGeorge syndrome, a review of 52 patients].
    Minier F; Carles D; Pelluard F; Alberti EM; Stern L; Saura R
    Arch Pediatr; 2005 Mar; 12(3):254-7. PubMed ID: 15734119
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
    Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
    Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
    [TBL] [Abstract][Full Text] [Related]  

  • 35. DiGeorge syndrome: clinical variability in a family with submicroscopic deletion at 22q11.2.
    Tsui KM; Ng YY; Lam TS
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(1):52-6. PubMed ID: 9066191
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
    Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J
    Am J Med Genet; 1994 Oct; 52(4):445-9. PubMed ID: 7747757
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.
    Rauch A; Hofbeck M; Leipold G; Klinge J; Trautmann U; Kirsch M; Singer H; Pfeiffer RA
    Am J Med Genet; 1998 Jul; 78(4):322-31. PubMed ID: 9714433
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Upper limb malformations in DiGeorge syndrome.
    Cormier-Daire V; Iserin L; Théophile D; Sidi D; Vervel C; Padovani JP; Vekemans M; Munnich A; Lyonnet S
    Am J Med Genet; 1995 Mar; 56(1):39-41. PubMed ID: 7747784
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Classical Noonan syndrome is not associated with deletions of 22q11.
    Robin NH; Sellinger B; McDonald-McGinn D; Zackai EH; Emanuel BS; Driscoll DA
    Am J Med Genet; 1995 Mar; 56(1):94-6. PubMed ID: 7747795
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 35.