BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 6604487)

  • 1. Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23).
    Solé MT; Rivera H; Sánchez-Corona J; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(2):120-2. PubMed ID: 6604487
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
    Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
    Kroyer S; Niebuhr E
    Ann Genet; 1975 Mar; 18(1):50-5. PubMed ID: 50043
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
    Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [De novo appearance of a partial trisomy 1q in mosaic due to a 1;9 translocation].
    Gagnon JA; Richer CL; Lemieux N; Gauthier-Chouinard M
    Ann Genet; 1984; 27(1):33-7. PubMed ID: 6609670
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F; Raoul O; Lescs MC; Danan C
    Am J Med Genet; 1985 Jul; 21(3):591-5. PubMed ID: 4025391
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM; Ferrari I
    Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotype.
    Van Buggenhout G; De Coen L; Fryns JP
    Ann Genet; 1998; 41(2):77-81. PubMed ID: 9706337
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood.
    Fryns JP; de Muelenaere A; Pedersen J; Van Den Berghe H
    Ann Genet; 1980; 23(3):181-2. PubMed ID: 6968537
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
    Ayraud N; Galiana A; Llyod M; Deswarte M
    Ann Genet; 1976 Mar; 19(1):65-8. PubMed ID: 1084126
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
    An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.
    Lapière JC; Verloes A; Herens C; Delfortrie J; Van Maldergem L; Gillerot Y; Koulischer L
    Genet Couns; 1992; 3(3):155-9. PubMed ID: 1388935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 22q12 leads to qter: "aneusomie de recombinaison" of a pericentric inversion.
    Cantu JM; Hernandez A; Vaca G; Plascencia L; Martinez-Basalo C; Ibarra B; Rivera H
    Ann Genet; 1981; 24(1):37-40. PubMed ID: 6971616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Asymmetric clinical and cytogenetic findings in a 4-year-old girl with trisomy 18 mosaicism.
    Rao KW; Buchanan PD; Aylsworth AS
    Birth Defects Orig Artic Ser; 1978; 14(6C):349-54. PubMed ID: 728589
    [No Abstract]   [Full Text] [Related]  

  • 19. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF; Wyandt H; Pan A; Milunsky JM
    Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
    Karamysheva TV; Matveeva VG; Shorina AP; Rubtsov NB
    Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.