BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 3963055)

  • 1. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA; Farag TI; Usha R; el-Khalifa MY; Sundareshan TS; Al-Othman SA
    Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B; Pilczer C; Dandine M; Tamboise A
    Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP; Heck LJ; Carter GA; Flom JO
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW; Chen H; Baucum RW; Hand AM
    Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
    Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo del(3)(q2800).
    Alvarez Arratia MC; Rivera H; Möller M; Valdivia A; Vigueras A; Cantu JM
    Ann Genet; 1984; 27(2):109-11. PubMed ID: 6331786
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Apparently nonmosaic trisomy 22: clinical report and review.
    Sundareshan TS; Naguib KK; al-Awadi SA; Redha MA; Hamoud MS
    Am J Med Genet; 1990 May; 36(1):7-10. PubMed ID: 2185636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).
    Benson K; Gordon M; Wassman ER; Tsi C
    Am J Med Genet; 1986 Nov; 25(3):405-11. PubMed ID: 3789004
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. 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]  

  • 14. Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies.
    Levin ML; Shaffer LG; Lewis RAp6 ; Gresik MV; Lupski JR
    Am J Med Genet; 1995 Jan; 55(1):30-2. PubMed ID: 7702093
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1q.
    Schinzel A
    Hum Genet; 1979 Jun; 49(2):167-73. PubMed ID: 468246
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS; Fidone GS; Reider-Garcia PA; Hansen KL; McCombs JL; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Infantile hemangioendothelioma of the liver in patient with interstitial deletion of chromosome 6q: report of an autopsy case.
    Ito H; Yamasaki T; Okamoto O; Tahara E
    Am J Med Genet; 1989 Nov; 34(3):325-9. PubMed ID: 2596522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).
    Al-Awadi SA; Farag TI; Naguib K; Teebi A; Cuschieri A; Al-Othman S; Sundareshan TS
    J Med Genet; 1983 Dec; 20(6):464-5. PubMed ID: 6655673
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 leads to 7p21.
    Miller M; Kaufman G; Reed G; Bilenker R; Schinzel A
    Am J Med Genet; 1979; 4(4):323-32. PubMed ID: 539602
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML; Ryan RM
    Am J Med Genet; 1995 Mar; 56(1):97-100. PubMed ID: 7747796
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.