BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 11693783)

  • 1. Terminal 6q25.3 deletion and abnormal behaviour.
    Lukusa T; Willekens D; Lukusa N; De Cock F; Fryns JP
    Genet Couns; 2001; 12(3):213-21. PubMed ID: 11693783
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG; Mingarelli R; Digilio MC; Zelante L; Giannotti A; Sabatino G; Dallapiccola B
    Ann Genet; 1992; 35(4):208-12. PubMed ID: 1296516
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
    de Almeida JC; Reis DF; Martins RR
    Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial monosomy 11q and trisomy 12q: variable expression in two siblings.
    Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP
    Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).
    Fryns JP; Kleczkowska A; Vogels A; Van den Berghe H
    Ann Genet; 1989; 32(3):171-3. PubMed ID: 2573313
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia.
    Magri C; Piovani G; Pilotta A; Michele T; Buzi F; Barlati S
    Eur J Med Genet; 2011; 54(3):361-4. PubMed ID: 21211576
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
    Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
    Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New insights into the phenotypes of 6q deletions.
    Hopkin RJ; Schorry E; Bofinger M; Milatovich A; Stern HJ; Jayne C; Saal HM
    Am J Med Genet; 1997 Jun; 70(4):377-86. PubMed ID: 9182778
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial 6q deletion: clinical and array CGH characterisation of a new patient.
    Le Caignec C; Swillen A; Van Asche E; Fryns JP; Vermeesch JR
    Eur J Med Genet; 2005; 48(3):339-45. PubMed ID: 16179229
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Proximal interstitial 6q deletion: a recognizable syndrome.
    Kumar R; Riordan D; Dawson AJ; Chudley AE
    Am J Med Genet; 1997 Aug; 71(3):353-6. PubMed ID: 9268108
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.
    Lukusa T; Smeets E; Vermeesch JR; Fryns JP
    Genet Couns; 2002; 13(4):417-25. PubMed ID: 12558112
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.
    Van Buggenhout G; Van Ravenswaaij-Arts C; Mc Maas N; Thoelen R; Vogels A; Smeets D; Salden I; Matthijs G; Fryns JP; Vermeesch JR
    Eur J Med Genet; 2005; 48(3):276-89. PubMed ID: 16179223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
    Rooms L; Reyniers E; Scheers S; van Luijk R; Wauters J; Van Aerschot L; Callaerts-Vegh Z; D'Hooge R; Mengus G; Davidson I; Courtens W; Kooy RF
    Eur J Hum Genet; 2006 Oct; 14(10):1090-6. PubMed ID: 16773126
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
    Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
    Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K; Páez MT; Kurosawa K; Yamamoto T
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
    Schinzel A; Binkert F; Lillington DM; Sands M; Stocks RJ; Lindenbaum RH; Matthews H; Sheridan H
    J Med Genet; 1991 May; 28(5):352-5. PubMed ID: 1865477
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes.
    Barajas-Barajas LO; Valdez LL; Gonzalez JR; García-García C; Rivera H; Ramírez L
    Genet Couns; 2004; 15(2):167-73. PubMed ID: 15287416
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy.
    Gibbons B; Tan SY; Tam PY
    Singapore Med J; 1999 Apr; 40(4):273-5. PubMed ID: 10487083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Provisional new syndrome of MR/MCA with evolving phenotype.
    Lacassie Y; Morava E; LaMotta I
    Am J Med Genet; 2002 Nov; 113(2):213-7. PubMed ID: 12407715
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.