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 *

187 related articles for article (PubMed ID: 3314663)

  • 21. Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidase.
    Frydman M; Steinberger J; Shabtai F; Steinherz R
    Am J Med Genet; 1986 Oct; 25(2):245-9. PubMed ID: 3096136
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
    Steinbach P; Wolf M; Schmidt H
    Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Interstitial deletion 11q. Case report and review of the literature.
    De Pater JM; Ippel PF; Bijlsma JB; Van Nieuwenhuizen O
    Genet Couns; 1997; 8(4):335-9. PubMed ID: 9457504
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Interstitial del(13q) associated with blindness and mental retardation.
    Juberg RC; Mowrey PN
    Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interstitial deletion (6)q13q15.
    Gershoni-Baruch R; Mandel H; Bar El H; Bar-Nizan N; Borochowitz Z; Dar H
    Am J Med Genet; 1996 Apr; 62(4):345-7. PubMed ID: 8723062
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Intercalary de novo deletion of chromosome 1: del(1) (q24 to q32)].
    Faugeras C; Barthe D
    J Genet Hum; 1985 Jan; 33(1):51-6. PubMed ID: 3981142
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients.
    Tranebjaerg L; Nielsen KB; Tommerup N; Warburg M; Mikkelsen M
    Am J Med Genet; 1988 Apr; 29(4):739-53. PubMed ID: 3400720
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Terminal deletion of the short arm of chromosome 3.
    Asai M; Ito Y; Iguchi T; Ito J; Okada N; Oishi H
    Jpn J Hum Genet; 1992 Jun; 37(2):163-8. PubMed ID: 1391972
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS; Golden WL
    Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.
    Keppen LD; Gollin SM; Edwards D; Sawyer J; Wilson W; Overhauser J
    Am J Med Genet; 1992 Oct; 44(3):356-60. PubMed ID: 1488985
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
    Gillar PJ; Kaye CI; Ryan SG; Moore CM
    Am J Med Genet; 1992 Sep; 44(2):138-41. PubMed ID: 1456281
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter.
    Telfer MA; Clark CE; Casey PA; Cowell HR; Stroud HH
    Clin Genet; 1980 Jun; 17(6):428-32. PubMed ID: 7398115
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.
    Yamamoto Y; Oguro N; Miyao M; Yanagisawa M
    Am J Med Genet; 1989 Jan; 32(1):133-5. PubMed ID: 2784939
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Interstitial deletion of long arm of chromosome 13.
    Carnevale A; Frias S; Alcantar R
    Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J; Voullaire L; Bankier A
    Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P; Vögtel D
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.