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 *

350 related articles for article (PubMed ID: 8696341)

  • 1. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.
    Daw SC; Taylor C; Kraman M; Call K; Mao J; Schuffenhauer S; Meitinger T; Lipson T; Goodship J; Scambler P
    Nat Genet; 1996 Aug; 13(4):458-60. PubMed ID: 8696341
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
    Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
    Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A
    Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
    Demczuk S; Aurias A
    Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.
    Yatsenko SA; Yatsenko AN; Szigeti K; Craigen WJ; Stankiewicz P; Cheung SW; Lupski JR
    Clin Genet; 2004 Aug; 66(2):128-36. PubMed ID: 15253763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Altered replication timing of the HIRA/Tuple1 locus in the DiGeorge and Velocardiofacial syndromes.
    D'Antoni S; Mattina T; Di Mare P; Federico C; Motta S; Saccone S
    Gene; 2004 May; 333():111-9. PubMed ID: 15177686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
    Lindsay EA; Halford S; Wadey R; Scambler PJ; Baldini A
    Genomics; 1993 Aug; 17(2):403-7. PubMed ID: 8406492
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).
    Schuffenhauer S; Lichtner P; Peykar-Derakhshandeh P; Murken J; Haas OA; Back E; Wolff G; Zabel B; Barisic I; Rauch A; Borochowitz Z; Dallapiccola B; Ross M; Meitinger T
    Eur J Hum Genet; 1998; 6(3):213-25. PubMed ID: 9781025
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
    Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
    McQuade L; Christodoulou J; Budarf M; Sachdev R; Wilson M; Emanuel B; Colley A
    Am J Med Genet; 1999 Sep; 86(1):27-33. PubMed ID: 10440825
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
    Funke B; Saint-Jore B; Puech A; Sirotkin H; Edelmann L; Carlson C; Raft S; Pandita RK; Kucherlapati R; Skoultchi A; Morrow BE
    Genomics; 1997 Dec; 46(3):364-72. PubMed ID: 9441739
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.
    Lipson A; Fagan K; Colley A; Colley P; Sholler G; Issacs D; Oates RK
    Am J Med Genet; 1996 Nov; 65(4):304-8. PubMed ID: 8923940
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome.
    Driscoll DA
    Methods Mol Med; 2006; 126():43-55. PubMed ID: 16930005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
    Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.
    Skrypnyk C; Goecke TO; Majewski F; Bartsch O
    Am J Med Genet; 2002 Nov; 113(2):207-12. PubMed ID: 12407714
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB; Chen E; Golabi M; Lebo RV
    Am J Med Genet; 1996 Dec; 66(3):250-6. PubMed ID: 8985481
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.
    Lichtner P; König R; Hasegawa T; Van Esch H; Meitinger T; Schuffenhauer S
    J Med Genet; 2000 Jan; 37(1):33-7. PubMed ID: 10633131
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.