BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 2185636)

  • 1. 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]  

  • 2. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E; Stetka DG
    Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy 22: no longer an enigma.
    Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
    Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature.
    Bacino CA; Schreck R; Fischel-Ghodsian N; Pepkowitz S; Prezant TR; Graham JM
    Am J Med Genet; 1995 May; 56(4):359-65. PubMed ID: 7604844
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternal origin and clinical findings in a case with trisomy 22.
    Mihçi E; Taçoy S; Yakut S; Ongun H; Keser I; Kiliçarslan B; Bağci G; Lüleci G
    Turk J Pediatr; 2007; 49(3):322-6. PubMed ID: 17990591
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
    Hou JW
    Chang Gung Med J; 2005 Sep; 28(9):657-61. PubMed ID: 16323558
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A; Allanson J; Crowe CA; Lipson MH; Johnson VP
    Am J Med Genet; 1992 Sep; 44(2):189-96. PubMed ID: 1456290
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial deletion of distal 17q.
    Bridge J; Sanger W; Mosher G; Buehler B; Nelson R; Welsh M; Newland J; Kafka M
    Am J Med Genet; 1985 Jun; 21(2):225-9. PubMed ID: 4014309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H; Zackai EH; Mellman WJ; Aronson M
    Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The 22q distal trisomy syndrome in a recombinant child.
    Rivera H; Garcia-Esquivel L; Romo MG; Perez-Garcia G; Martinez y Martinez R
    Ann Genet; 1988; 31(1):47-9. PubMed ID: 3258493
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG; Zackowski JL; Storto PD; Newlin A
    Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A new case of trisomy 5p].
    Antonenko VG; Levina LIa; Chudnova VI
    Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The trisomy 9p syndrome.
    Centerwall WR; Beatty-DeSana JW
    Pediatrics; 1975 Nov; 56(5):748-55. PubMed ID: 1196731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA; Higgins RR
    Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature.
    Cantú ES; Eicher DJ; Pai GS; Donahue CJ; Harley RA
    Am J Med Genet; 1996 Apr; 62(4):330-5. PubMed ID: 8723059
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The syndrome of ring chromosome 12.
    Scribanu N; McCullars EB; Baumiller RC; Colon AR
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.