BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 9497944)

  • 21. Scoliosis in velo-cardio-facial syndrome.
    Morava E; Lacassie Y; King A; Illes T; Marble M
    J Pediatr Orthop; 2002; 22(6):780-3. PubMed ID: 12409907
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
    Tsai CH; Van Dyke DL; Feldman GL
    Am J Med Genet; 1999 Feb; 82(4):336-9. PubMed ID: 10051168
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome].
    Somer M; Ignatius J; Vehmanen P; Keinänen M; Haapanen ML
    Duodecim; 1997; 113(12):1115-22. PubMed ID: 11466836
    [No Abstract]   [Full Text] [Related]  

  • 24. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
    Vaz SO; Pires R; Pires LM; Carreira IM; Anjos R; Maciel P; Mota-Vieira L
    BMC Pediatr; 2015 Aug; 15():95. PubMed ID: 26297018
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G; Bartmus D; Bartels I
    Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
    [No Abstract]   [Full Text] [Related]  

  • 26. Phenotype of adults with the 22q11 deletion syndrome: A review.
    Cohen E; Chow EW; Weksberg R; Bassett AS
    Am J Med Genet; 1999 Oct; 86(4):359-65. PubMed ID: 10494092
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?
    Worthington S; Colley A; Fagan K; Dai K; Lipson AH
    J Med Genet; 1997 Jan; 34(1):79-82. PubMed ID: 9032655
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Presenting phenotype in 100 children with the 22q11 deletion syndrome.
    Oskarsdóttir S; Persson C; Eriksson BO; Fasth A
    Eur J Pediatr; 2005 Mar; 164(3):146-53. PubMed ID: 15565286
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.
    Pragliola A; Jurecic V; Chau CK; Philip N; Baldini A
    Am J Hum Genet; 1997 Dec; 61(6):1456-9. PubMed ID: 9399910
    [No Abstract]   [Full Text] [Related]  

  • 30. Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study.
    Friedman MA; Miletta N; Roe C; Wang D; Morrow BE; Kates WR; Higgins AM; Shprintzen RJ
    Int J Pediatr Otorhinolaryngol; 2011 Sep; 75(9):1167-72. PubMed ID: 21763005
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
    Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gastrointestinal tract anomalies in velocardiofacial syndrome.
    Enns GM; Cox VA; Golabi M; Immken L; Fisher J; Curry C
    Am J Med Genet; 1999 Jun; 84(4):382-3. PubMed ID: 10340658
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Malocclusions and craniofacial anomalies in a child with velo-cardio-facial syndrome.
    Matthews-Brzozowska T; Baranowska J; Rogiński P; Obersztyn E; Cudziło D
    Dev Period Med; 2015; 19(4):490-5. PubMed ID: 26982759
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
    Ford LC; Sulprizio SL; Rasgon BM
    Laryngoscope; 2000 Mar; 110(3 Pt 1):362-7. PubMed ID: 10718420
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).
    Antshel KM; Conchelos J; Lanzetta G; Fremont W; Kates WR
    Psychiatry Res; 2005 Apr; 138(3):235-45. PubMed ID: 15854791
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.