BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

532 related articles for article (PubMed ID: 7573155)

  • 1. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neuroblastoma in patients with constitutional chromosomal changes.
    Fryns JP
    Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause.
    Coco R; Penchaszadeh VB
    Am J Med Genet; 1982 Jun; 12(2):155-73. PubMed ID: 7102722
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
    Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [11q distal trisomy due to a familial 11;18 translocation].
    Menéndez I; Rivera H; Morales E; Juan J; Jiménez M
    Bol Med Hosp Infant Mex; 1990 Nov; 47(11):792-4. PubMed ID: 2285470
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA; Stevens MA; Byrne-Essif K; Cassidy SB
    Am J Med Genet; 1992 Sep; 44(1):18-23. PubMed ID: 1519644
    [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. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rieger syndrome and interstitial 4q26 deletion.
    Fryns JP; Van Den Berghe H
    Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
    [No Abstract]   [Full Text] [Related]  

  • 14. A patient with partial duplication 2q and partial deficiency 11q.
    Ho CK; Henderson KC; Bowyer FP; Eilers KB; Andrews LG
    Am J Med Genet; 1987 Nov; 28(3):575-9. PubMed ID: 3322008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
    Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS
    Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year].
    Chrzanowska K; Fryns JP
    J Genet Hum; 1989 Sep; 37(3):259-61. PubMed ID: 2625629
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU; Baumann WA
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
    Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.