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 *

187 related articles for article (PubMed ID: 8618195)

  • 21. [Microdeletion 22q11.2. A too rarely diagnosed genetic change in psychiatric illnesses].
    Leyhe T; Haarmeier T; Dufke A; Giedke H
    Nervenarzt; 2002 May; 73(5):452-7. PubMed ID: 12078024
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
    Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
    Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Hypoparathyroidism associated with aneurysm of the left subclavian artery (Kommerell's diverticulum) in an adult patient with a chromosome 22q11.2 deletion.
    Trombetti A; Bottani A; George F; Rizzoli R
    J Bone Miner Res; 2001 Oct; 16(10):1926-8. PubMed ID: 11585359
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Growth characteristics and endocrine abnormalities in 22q11.2 deletion syndrome.
    Levy-Shraga Y; Gothelf D; Goichberg Z; Katz U; Somech R; Pinhas-Hamiel O; Modan-Moses D
    Am J Med Genet A; 2017 May; 173(5):1301-1308. PubMed ID: 28421700
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial (Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2.
    Fokstuen S; Vrticka K; Riegel M; Da Silva V; Baumer A; Schinzel A
    Eur J Pediatr; 2001 Jan; 160(1):54-7. PubMed ID: 11195019
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.
    Motzkin B; Marion R; Goldberg R; Shprintzen R; Saenger P
    J Pediatr; 1993 Sep; 123(3):406-10. PubMed ID: 8355116
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complex conotruncal heart defect, severe bleeding disorder and 22q11 deletion: a new case of Bernard-Soulier syndrome and of 22q11 deletion syndrome?
    Iascone MR; Sacchelli M; Vittorini S; Giusti S
    Ital Heart J; 2001 Jun; 2(6):475-7. PubMed ID: 11453587
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Renal malformations in deletion 22q11.2 patients.
    Kujat A; Schulz MD; Strenge S; Froster UG
    Am J Med Genet A; 2006 Jul; 140(14):1601-2. PubMed ID: 16761295
    [No Abstract]   [Full Text] [Related]  

  • 32. Screening of patients at risk for 22q11 deletion.
    Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
    Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Kousseff syndrome caused by deletion of chromosome 22q11-13.
    Forrester S; Kovach MJ; Smith RE; Rimer L; Wesson M; Kimonis VE
    Am J Med Genet; 2002 Nov; 112(4):338-42. PubMed ID: 12376934
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome.
    Lima K; Abrahamsen TG; Wolff AB; Husebye E; Alimohammadi M; Kämpe O; Følling I
    Eur J Endocrinol; 2011 Aug; 165(2):345-52. PubMed ID: 21606191
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome.
    Sandrin-Garcia P; Macedo C; Martelli LR; Ramos ES; Guion-Almeida ML; Richieri-Costa A; Passos GA
    Clin Genet; 2002 May; 61(5):380-3. PubMed ID: 12081724
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
    Lindsay EA; Greenberg F; Shaffer LG; Shapira SK; Scambler PJ; Baldini A
    Am J Med Genet; 1995 Mar; 56(2):191-7. PubMed ID: 7625444
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Radial aplasia and chromosome 22q11 deletion.
    Digilio MC; Giannotti A; Marino B; Guadagni AM; Orzalesi M; Dallapiccola B
    J Med Genet; 1997 Nov; 34(11):942-4. PubMed ID: 9391893
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.