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 *

356 related articles for article (PubMed ID: 8946108)

  • 21. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients.
    Borgmann S; Luhmer I; Arslan-Kirchner M; Kallfelz HC; Schmidtke J
    Eur J Pediatr; 1999 Dec; 158(12):958-63. PubMed ID: 10592069
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. The search for hemizygosity at 22qll in patients with isolated cleft palate.
    Mingarelli R; Digilio MC; Mari A; Amati F; Standoli L; Giannotti A; Novelli G; Dallapiccola B
    J Craniofac Genet Dev Biol; 1996; 16(2):118-21. PubMed ID: 8773902
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.
    Driscoll DA; Spinner NB; Budarf ML; McDonald-McGinn DM; Zackai EH; Goldberg RB; Shprintzen RJ; Saal HM; Zonana J; Jones MC
    Am J Med Genet; 1992 Sep; 44(2):261-8. PubMed ID: 1360769
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
    Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS
    J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome.
    Saitta SC; Harris SE; McDonald-McGinn DM; Emanuel BS; Tonnesen MK; Zackai EH; Seitz SC; Driscoll DA
    Am J Med Genet A; 2004 Jan; 124A(3):313-7. PubMed ID: 14708107
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [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]  

  • 34. Velo-cardio-facial syndrome: a review of 120 patients.
    Goldberg R; Motzkin B; Marion R; Scambler PJ; Shprintzen RJ
    Am J Med Genet; 1993 Feb; 45(3):313-9. PubMed ID: 8434617
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.
    Portnoï MF; Lebas F; Gruchy N; Ardalan A; Biran-Mucignat V; Malan V; Finkel L; Roger G; Ducrocq S; Gold F; Taillemite JL; Marlin S
    Am J Med Genet A; 2005 Aug; 137(1):47-51. PubMed ID: 16007629
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Monozygotic twins with 22q11 deletion and discordant phenotypes.
    Fryer A
    J Med Genet; 1996 Feb; 33(2):173. PubMed ID: 8929959
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. [Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].
    Doray B; Badila-Timbolschi D; Schaefer E; Fattori D; Monga B; Dott B; Favre R; Kohler M; Nisand I; Viville B; Kauffmann I; Bruant-Rodier C; Grollemund B; Rinkenbach R; Astruc D; Gasser B; Lindner V; Marcellin L; Flori E; Girard-Lemaire F; Dollfus H
    Arch Pediatr; 2012 Oct; 19(10):1021-9. PubMed ID: 22925539
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 18.