BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

816 related articles for article (PubMed ID: 10528241)

  • 1. 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]  

  • 2. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Report of two cases of distal deletion of the long arm of chromosome 6.
    Stevens CA; Fineman RM; Breg WR; Silken AB
    Am J Med Genet; 1988 Apr; 29(4):807-14. PubMed ID: 3400725
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
    Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
    Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
    Gorski JL; Uhlmann WR; Glover TW
    Am J Med Genet; 1990 Dec; 37(4):471-4. PubMed ID: 2260590
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
    Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
    Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL; Duncan AM; Khalifa MM
    Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome 6q deletions: a report of two additional cases and a review of the literature.
    McLeod DR; Fowlow SB; Robertson A; Samcoe D; Burgess I; Hoo JJ
    Am J Med Genet; 1990 Jan; 35(1):79-84. PubMed ID: 2405671
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies.
    Werner W; Kraft S; Callen DF; Bartsch O; Hinkel GK
    Am J Med Genet; 1997 Jun; 70(4):371-6. PubMed ID: 9182777
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo interstitial deletion q16.2q21 on chromosome 6.
    Villa A; Urioste M; Bofarull JM; Martínez-Frías ML
    Am J Med Genet; 1995 Jan; 55(3):379-83. PubMed ID: 7726240
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
    Mattia FR; Wardinsky TD; Tuttle DJ; Grix A; Smith KA; Walling P
    Am J Med Genet; 1992 Nov; 44(5):551-4. PubMed ID: 1481806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interstitial deletion del(10)(q25.2q25.3 approximately 26.11)--case report and review of the literature.
    Kehrer-Sawatzki H; Daumiller E; Müller-Navia J; Kendziorra H; Rossier E; du Bois G; Barbi G
    Prenat Diagn; 2005 Oct; 25(10):954-9. PubMed ID: 16088867
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
    Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA; Albertson DG; Pinkel D; Cotter PD
    Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S; del Rey G; Heinrich J; Coco R
    Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 41.