BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 4140832)

  • 1. Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.
    de Grouchy J; Turleau C
    Humangenetik; 1974; 24(3):197-200. PubMed ID: 4140832
    [No Abstract]   [Full Text] [Related]  

  • 2. [Probable localisation of a Hageman (factor XII) locus on an autosome].
    Josso F; de Grouchy J
    Ann Genet; 1968 Jun; 11(2):95-7. PubMed ID: 5303429
    [No Abstract]   [Full Text] [Related]  

  • 3. Hageman (factor XII) locus on 7q?: report of a second case with del(7)q35 and normal factor XII level.
    Francke U
    Hum Genet; 1978 Dec; 45(3):363-7. PubMed ID: 738736
    [No Abstract]   [Full Text] [Related]  

  • 4. Two cases with different deletions of the long arm of chromosome 7.
    Klep-de Pater JM; Bijlsma JB; Bleeker-Wagemakers EM; de France HF; de Vries-Ekkers CM
    J Med Genet; 1979 Apr; 16(2):151-4. PubMed ID: 458833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7.
    Biederman B; Bowen P
    Hum Genet; 1978 Feb; 41(1):101-7. PubMed ID: 631854
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial study in congenital Hageman factor deficiency (blood coagulation factor XII)].
    Baumann R; Straub PW
    Schweiz Med Wochenschr; 1968 Oct; 98(42):1653-5. PubMed ID: 5698343
    [No Abstract]   [Full Text] [Related]  

  • 9. 7qter deletion with normal Hageman factor.
    Kawashima H; Taniguchi N
    Jinrui Idengaku Zasshi; 1981 Sep; 26(3):249-53. PubMed ID: 7334693
    [No Abstract]   [Full Text] [Related]  

  • 10. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
    Hobolth N; Jacobsen P; Mikkelsen M
    J Med Genet; 1974 Sep; 11(3):299-303. PubMed ID: 4139263
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH; Broske SP; Moore CM; Thomas GH; Neill CA
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Normal Hageman factor level in 7q deletion syndrome.
    Kawashima H; Taniguchi N
    Clin Genet; 1981 Mar; 19(3):207-8. PubMed ID: 7273466
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O; Yunis JJ; Escobar JI
    Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP; Kleczkowska A; van den Berghe H
    Clin Genet; 1988 Jan; 33(1):60-2. PubMed ID: 3342549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Two unrelated children with distal long arm deletion of chromosome 7: clinical features, cytogenetic and gene marker studies.
    Bernstein R; Dawson B; Morcom G; Wagner J; Jenkins T
    Clin Genet; 1980; 17(3):228-37. PubMed ID: 6928813
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.