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 *

100 related articles for article (PubMed ID: 9375730)

  • 1. De novo 16p deletion: ATR-16 syndrome.
    Lindor NM; Valdes MG; Wick M; Thibodeau SN; Jalal S
    Am J Med Genet; 1997 Nov; 72(4):451-4. PubMed ID: 9375730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ATR-16 due to a de novo complex rearrangement of chromosome 16.
    Gallego MS; Zelaya G; Feliu AS; Rossetti L; Shaffer LG; Bailey KA; Bacino CA; Barreiro CZ
    Hemoglobin; 2005; 29(2):141-50. PubMed ID: 15921166
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome.
    Pfeifer D; Poulat F; Holinski-Feder E; Kooy F; Scherer G
    Genomics; 2000 Jan; 63(1):108-16. PubMed ID: 10662550
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refinement of the genetic cause of ATR-16.
    Harteveld CL; Kriek M; Bijlsma EK; Erjavec Z; Balak D; Phylipsen M; Voskamp A; di Capua E; White SJ; Giordano PC
    Hum Genet; 2007 Nov; 122(3-4):283-92. PubMed ID: 17598130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).
    Lamb J; Harris PC; Wilkie AO; Wood WG; Dauwerse JG; Higgs DR
    Am J Hum Genet; 1993 Apr; 52(4):668-76. PubMed ID: 8460633
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial adenomatous polyposis and mental retardation caused by a de novo chromosomal deletion at 5q15-q22: report of a case.
    Finch R; Moore HG; Lindor N; Jalal SM; Markowitz A; Suresh J; Offit K; Guillem JG
    Dis Colon Rectum; 2005 Nov; 48(11):2148-52. PubMed ID: 16228830
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
    Gibbons RJ; Brueton L; Buckle VJ; Burn J; Clayton-Smith J; Davison BC; Gardner RJ; Homfray T; Kearney L; Kingston HM
    Am J Med Genet; 1995 Jan; 55(3):288-99. PubMed ID: 7726225
    [TBL] [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. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
    Reardon W; Gibbons RJ; Winter RM; Baraitser M
    Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: a new kindred with severe genital anomalies and mild hematologic expression.
    McPherson EW; Clemens MM; Gibbons RJ; Higgs DR
    Am J Med Genet; 1995 Jan; 55(3):302-6. PubMed ID: 7726227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
    J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.
    Lespinasse J; Gimelli S; Béna F; Antonarakis SE; Ansermet F; Paoloni-Giacobino A
    Eur J Med Genet; 2009; 52(1):49-52. PubMed ID: 18992376
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.
    Lefort G; Taib J; Toutain A; Houdayer C; Moraine CI; Humeau C; Sarda P
    Ann Genet; 1993; 36(4):200-5. PubMed ID: 8166424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
    BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome].
    Kurosawa K
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):824-5. PubMed ID: 11529043
    [No Abstract]   [Full Text] [Related]  

  • 18. A case with de novo interstitial deletion of chromosome 7q21.1-q22.
    Manguoğlu E; Berker-Karaüzüm S; Baumer A; Mihçi E; Taçoy S; Lüleci G; Schinzel A
    Genet Couns; 2005; 16(2):155-9. PubMed ID: 16080295
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.
    Wuyts W; Roland D; Lüdecke HJ; Wauters J; Foulon M; Van Hul W; Van Maldergem L
    Am J Med Genet; 2002 Dec; 113(4):326-32. PubMed ID: 12457403
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical manifestations of chromosome 21 interstitial deletion: report of four cases.
    Su PH; Chen JY; Chen SJ; Lin LL
    Acta Paediatr Taiwan; 2006; 47(6):303-8. PubMed ID: 17407982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.