These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 6725006)

  • 1. Trisomy 4q31----qter due to a maternal 4/8 translocation.
    Annerén G; Lübeck PO
    Hereditas; 1984; 100(1):45-9. PubMed ID: 6725006
    [No Abstract]   [Full Text] [Related]  

  • 2. [Partial trisomy for the segment 21(q11----qter) resulting from a de novo translocation between chromosomes 5 and 21].
    Crippa L; Ballaman J; Engel E
    Ann Genet; 1984; 27(3):190-3. PubMed ID: 6239590
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling].
    Ballesta F; Fernández E; Milá M
    J Genet Hum; 1980 Sep; 28(3):361-6. PubMed ID: 7463035
    [No Abstract]   [Full Text] [Related]  

  • 4. Trisomy 11q(q21 leads to qter).
    Bader PI; Jansch M; Hoffman D; Palmer CG; Gerber H; Taylor G
    Birth Defects Orig Artic Ser; 1978; 14(6C):383-92. PubMed ID: 728594
    [No Abstract]   [Full Text] [Related]  

  • 5. [Trisomy 11qter(11q21 and 11q23----qter) syndrome. Presentation of a case with familial translocation t(11;12) (q23,1----qter;q24,3)].
    Vianello MG; Chiossi F; Fasce L; Besio B; Chiossi M
    Minerva Pediatr; 1986 Mar; 38(5-6):183-92. PubMed ID: 3724715
    [No Abstract]   [Full Text] [Related]  

  • 6. A malformed newborn with 9p and 4q trisomy.
    Fryns JP; Azou M; Devliegher H; Eggermont E; van den Berghe H
    Ann Genet; 1981; 24(1):48-50. PubMed ID: 6971619
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial translocation t(8;14) with a case of tertiary trisomy, +14q-.
    Soudek D; Hunter P; O'Shaughnessy S; Simpson NE; Soudek V
    Birth Defects Orig Artic Ser; 1978; 14(6C):309-15. PubMed ID: 728586
    [No Abstract]   [Full Text] [Related]  

  • 8. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J
    J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
    Martin-Lucas MA; Pérez-Castillo A; Abrisqueta JA; de Torres ML; Martin-Sempere MJ; Del Mazo J; Aller V
    Ann Genet; 1982; 25(3):172-8. PubMed ID: 6982670
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS; Lewis FJ; Vowles M
    J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Translocation t(11;14) and trisomy 11q13----qter in multiple myeloma.
    Venti G; Mecucci C; Donti E; Tabilio A
    Ann Genet; 1984; 27(1):53-5. PubMed ID: 6609674
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial trisomy 12q24.31----qter.
    Tajara EH; Varella-Garcia M; Gusson AC
    J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
    Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 9p due to a maternal complex translocation involving chromosomes 4, 6 and 9.
    Tanaka N; Ikeuchi T; Yara I; Kitahara K
    Jinrui Idengaku Zasshi; 1977 Mar; 21(4):261-8. PubMed ID: 559818
    [No Abstract]   [Full Text] [Related]  

  • 15. Partial trisomy 5q: three different phenotypes depending on different duplication segments.
    Rodewald A; Zankl M; Gley EO; Zang KD
    Hum Genet; 1980; 55(2):191-8. PubMed ID: 7450763
    [No Abstract]   [Full Text] [Related]  

  • 16. [2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].
    Aurias A; Turc C; Michiels Y; Sinet PM; Graveleau D; Lejeune J
    Ann Genet; 1975 Sep; 18(3):185-8. PubMed ID: 1080981
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome level.
    Cantu JM; Hernandez A; Nazara Z; Rolon A; Ramirez ML; Sanchez-Corona J; Rivera H
    Ann Genet; 1981; 24(1):41-4. PubMed ID: 6971617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Translocation (3;12) (p21-pter; q24.1-qter) and phenylketonuria.
    Ganguly BB; Dalvi R; Mehta AV
    Cytobios; 2001; 106(411):63-70. PubMed ID: 11478664
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two sibs with duplication of 4q31-->qter due to 3:1 meiotic disjunction and mild phenotype.
    Moreira LM; Riegel M
    Genet Couns; 2000; 11(3):249-59. PubMed ID: 11043433
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.