BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 8792822)

  • 1. A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.
    Davies AF; Olavesen MG; Stephens RJ; Davidson R; Delneste D; Van Regemorter N; Vamos E; Flinter F; Abusaad I; Ragoussis J
    Hum Genet; 1996 Oct; 98(4):454-9. PubMed ID: 8792822
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Delineation of two distinct 6p deletion syndromes.
    Davies AF; Mirza G; Sekhon G; Turnpenny P; Leroy F; Speleman F; Law C; van Regemorter N; Vamos E; Flinter F; Ragoussis J
    Hum Genet; 1999 Jan; 104(1):64-72. PubMed ID: 10071194
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes.
    Mirza G; Williams RR; Mohammed S; Clark R; Newbury-Ecob R; Baldinger S; Flinter F; Ragoussis J
    Eur J Hum Genet; 2004 Sep; 12(9):718-28. PubMed ID: 15150541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
    Descipio C; Schneider L; Young TL; Wasserman N; Yaeger D; Lu F; Wheeler PG; Williams MS; Bason L; Jukofsky L; Menon A; Geschwindt R; Chudley AE; Saraiva J; Schinzel AA; Guichet A; Dobyns WE; Toutain A; Spinner NB; Krantz ID
    Am J Med Genet A; 2005 Apr; 134A(1):3-11. PubMed ID: 15704124
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3.
    Garcia-Miñaur S; Ramsay J; Grace E; Minns RA; Myles LM; FitzPatrick DR
    Am J Med Genet A; 2005 Feb; 132A(4):402-10. PubMed ID: 15742475
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
    Vermeesch JR; Fryns JP
    Am J Med Genet A; 2003 Jul; 120A(2):299-300. PubMed ID: 12833421
    [No Abstract]   [Full Text] [Related]  

  • 8. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.
    Zollino M; Di Stefano C; Zampino G; Mastroiacovo P; Wright TJ; Sorge G; Selicorni A; Tenconi R; Zappalà A; Battaglia A; Di Rocco M; Palka G; Pallotta R; Altherr MR; Neri G
    Am J Med Genet; 2000 Sep; 94(3):254-61. PubMed ID: 10995514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Schizophrenia in an adult with 6p25 deletion syndrome.
    Caluseriu O; Mirza G; Ragoussis J; Chow EW; MacCrimmon D; Bassett AS
    Am J Med Genet A; 2006 Jun; 140(11):1208-13. PubMed ID: 16642507
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.
    Martinet D; Filges I; Besuchet Schmutz N; Morris MA; Gaide AC; Dahoun S; Bottani A; Addor MC; Antonarakis SE; Beckmann JS; Béna F
    Am J Med Genet A; 2008 Aug; 146A(16):2094-102. PubMed ID: 18629875
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases.
    Le Caignec C; De Mas P; Vincent MC; Bocéno M; Bourrouillou G; Rival JM; David A
    Am J Med Genet A; 2005 Jan; 132A(2):175-80. PubMed ID: 15578619
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.
    Tomkins DJ; Hunter AG; Uchida IA; Roberts MH
    Clin Genet; 1982 Dec; 22(6):348-55. PubMed ID: 7160106
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A; Cain R; Howell R
    Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.
    Becker SA; Popp S; Rager K; Jauch A
    Eur J Pediatr; 2003 Apr; 162(4):267-70. PubMed ID: 12647202
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
    Callen DF; Eyre H; Lane S; Shen Y; Hansmann I; Spinner N; Zackai E; McDonald-McGinn D; Schuffenhauer S; Wauters J
    J Med Genet; 1993 Oct; 30(10):828-32. PubMed ID: 8230159
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases.
    Irving M; Hanson H; Turnpenny P; Brewer C; Ogilvie CM; Davies A; Berg J
    Am J Med Genet A; 2003 Dec; 123A(2):153-63. PubMed ID: 14598339
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.
    Devriendt K; Matthijs G; Van Dael R; Gewillig M; Eyskens B; Hjalgrim H; Dolmer B; McGaughran J; Bröndum-Nielsen K; Marynen P; Fryns JP; Vermeesch JR
    Am J Hum Genet; 1999 Apr; 64(4):1119-26. PubMed ID: 10090897
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.