BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 4811755)

  • 1. Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.
    Mayeda K; Weiss L; Lindahl R; Dully M
    Am J Hum Genet; 1974 Jan; 26(1):59-64. PubMed ID: 4811755
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
    Rosenthal IM; Krmpotic E; Bocian M; Szego K
    Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
    [No Abstract]   [Full Text] [Related]  

  • 3. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 4. A family showing transmission of a translocation t(3porq-;Cq+).
    McHugh J; Wright T; Cooke P
    J Med Genet; 1971 Dec; 8(4):509-12. PubMed ID: 5149535
    [No Abstract]   [Full Text] [Related]  

  • 5. [Pallister-Killian syndrome and 12p tetrasomy: increased LDH-B activity].
    Antich Femenias J; Briones Godino MP; Vilaseca Busca MA; Girós Blasco ML; Campos Castelló J; Jaume Roig B; Clusellas Casals N
    An Esp Pediatr; 1991 Jun; 34(6):459-62. PubMed ID: 1929015
    [No Abstract]   [Full Text] [Related]  

  • 6. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 7. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
    Mikkelsen M; Dahl G
    Cytogenet Cell Genet; 1973; 12(5):357-66. PubMed ID: 4131091
    [No Abstract]   [Full Text] [Related]  

  • 8. A ring-20 chromosome.
    Atkins L; Miller WL; Salam M
    J Med Genet; 1972 Sep; 9(3):377-80. PubMed ID: 4627939
    [No Abstract]   [Full Text] [Related]  

  • 9. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
    del Solar C; Uchida IA
    J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
    [No Abstract]   [Full Text] [Related]  

  • 10. Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomes.
    Breg WR; Alderdice PW; Miller DA; Miller OJ
    Nat New Biol; 1972 Mar; 236(64):76-8. PubMed ID: 4502457
    [No Abstract]   [Full Text] [Related]  

  • 11. [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].
    Rethoré MO; Kaplan JC; Junien C; Cruveiller J; Dutrillaux B; Aurias A; Carpentier S; Lafourcade J; Lejeune
    Ann Genet; 1975 Jun; 18(2):81-7. PubMed ID: 1081369
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mental deficiency and malformations in a boy with a group-C ring chromosome: 46, XY, Cr.
    Wurster D; Pomeroy J; Benirschke K; Hoefnagel D
    J Ment Defic Res; 1969 Sep; 13(3):184-90. PubMed ID: 5823674
    [No Abstract]   [Full Text] [Related]  

  • 13. A case of partial trisomy 10q.
    Laća Z; Kalicanin P
    J Ment Defic Res; 1974 Dec; 18(4):285-91. PubMed ID: 4465466
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF; Weber F; Muller HM; Burwell JK
    Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
    [No Abstract]   [Full Text] [Related]  

  • 15. Cytogenetic study of a 5-14 translocation in man.
    Borgaonkar DS; Blair SM; Lutz JB; Kelly T; Tice RR; Delaney NV; Hutchinson JR; Bias WB
    J Hered; 1973; 64(5):299-300. PubMed ID: 4782671
    [No Abstract]   [Full Text] [Related]  

  • 16. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Jacobsen P; Mikkelsen M; Rosleff F
    Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
    [No Abstract]   [Full Text] [Related]  

  • 17. A malformed girl with duplication of chromosome 9q.
    Nakahori Y; Nakagome Y
    J Med Genet; 1984 Oct; 21(5):387-8. PubMed ID: 6502654
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial mental retardation in a family with an inherited chromosome rearrangement.
    Chudley AE; Bauder F; Ray M; McAlpine PJ; Pena SD; Hamerton JL
    J Med Genet; 1974 Dec; 11(4):353-66. PubMed ID: 4140909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ring chromosome 7 with variable phenotypic expression.
    Zackai EH; Breg WR
    Cytogenet Cell Genet; 1973; 12(1):40-8. PubMed ID: 4145271
    [No Abstract]   [Full Text] [Related]  

  • 20. SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214).
    Leschot NJ; Slater RM; Joenje H; Becker-Bloemkolk MJ; de Nef JJ
    Hum Genet; 1981; 57(2):220-3. PubMed ID: 7228038
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.