BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 7188997)

  • 1. [Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)].
    Kessel E; Pfeiffer RA; Baisch C
    Klin Padiatr; 1980 Jan; 192(1):85-90. PubMed ID: 7188997
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS; Summitt RL; Martens P; Gooch WM
    Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
    Fryns JP; Kleczkowska A; Decock P; Van den Berghe H
    Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 15q: report of a patient and literature review.
    Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
    Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
    Kessel E; Pfeiffer RA; Kosenow W
    Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC
    Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inherited partial trisomy 2: 46,XX,1p+;t(1;2) (p36;q31).
    Warren RJ; Panizales EG; Cantwell RJ
    Birth Defects Orig Artic Ser; 1975; 11(5):177-9. PubMed ID: 1218210
    [No Abstract]   [Full Text] [Related]  

  • 11. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
    Coco R; Penchaszadeh VB
    J Genet Hum; 1978 Sep; 26(3):203-10. PubMed ID: 739260
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Cp trisomy: a new syndrome].
    Canu JM; Buentello L; Armendares S
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract]   [Full Text] [Related]  

  • 14. [Ring chromosome D13-case history and survey (author's transl)].
    Zink U; Rix R; Grosse KP; Schwanitz G
    Klin Padiatr; 1973 May; 185(3):192-7. PubMed ID: 4795573
    [No Abstract]   [Full Text] [Related]  

  • 15. [Distal trisomy 14q caused by a paternal translocation (6;14)].
    Velasco F; Clusellas N; Godo RM; Antich J
    An Esp Pediatr; 1984 Nov; 21(7):681-7. PubMed ID: 6524780
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
    Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ["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]  

  • 19. 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]  

  • 20. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
    Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.