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 *

134 related articles for article (PubMed ID: 5698839)

  • 1. MN blood-group locus: data concerning the possible chromosomal location.
    German J; Walker ME; Stiefel FH; Allen FH
    Science; 1968 Nov; 162(3857):1014-5. PubMed ID: 5698839
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autoradiographic studies of human chromosomes. II. Data concerning the position of the MN locus.
    German JL; Walker ME; Stiefel FH; Allen FH
    Vox Sang; 1969 Feb; 16(2):130-45. PubMed ID: 5766881
    [No Abstract]   [Full Text] [Related]  

  • 3. [Abnormal C group chromosome in several members of the same family].
    Emerit I; Vernant P
    Humangenetik; 1968; 6(4):326-34. PubMed ID: 5713618
    [No Abstract]   [Full Text] [Related]  

  • 4. Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.
    Genest P; Lachance R; Poty J; Jacob D
    J Med Genet; 1971 Dec; 8(4):504-8. PubMed ID: 5149534
    [No Abstract]   [Full Text] [Related]  

  • 5. Deletion of the long arm of chromosome no. 7: tentative assignment of the Kidd (Jk) locus.
    Shokeir MH; Ying KL; Pabello P
    Clin Genet; 1973; 4(4):360-8. PubMed ID: 4518278
    [No Abstract]   [Full Text] [Related]  

  • 6. Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
    Reiss JA; Wyandt HE; Magenis RE; Lovrien EW; Hecht F
    J Med Genet; 1972 Sep; 9(3):280-6. PubMed ID: 5079098
    [No Abstract]   [Full Text] [Related]  

  • 7. [Deficiency in the short arms of Group B (4p--; 5p--) chromosomes. Studies on 6 patients].
    Altrogge HC; Hirth L; Goedde HW; Schroeder HJ
    Z Kinderheilkd; 1971; 110(3):218-47. PubMed ID: 5088755
    [No Abstract]   [Full Text] [Related]  

  • 8. Inherited t(13q14q) in two retarded sisters.
    Crandall BF; Francke U; Campbell MA; Sparkes RS
    Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
    [No Abstract]   [Full Text] [Related]  

  • 9. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
    Wyandt HE; Hecht F; Lovrien EW; Stewart RE
    Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418
    [No Abstract]   [Full Text] [Related]  

  • 10. Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies.
    Jacobsen P; Mikkelsen M; Froland A; Dupont A
    Ann Hum Genet; 1966 May; 29(4):391-402. PubMed ID: 5961828
    [No Abstract]   [Full Text] [Related]  

  • 11. [Clinical and cytogenetic findings in a rare autosomal aberrations].
    Tolksdorf M
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):308-13. PubMed ID: 5523669
    [No Abstract]   [Full Text] [Related]  

  • 12. A human ring C chromosome associated with multiple congenital abnormalities.
    De Chieri PR; Albores JM; Cosín A; Cosín JM
    J Med Genet; 1972 Jun; 9(2):239-42. PubMed ID: 5046637
    [No Abstract]   [Full Text] [Related]  

  • 13. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders. I. Cases 1 and 2.
    Moore MK; Engel E
    Ann Genet; 1969 Dec; 12(4):265-9. PubMed ID: 5309420
    [No Abstract]   [Full Text] [Related]  

  • 14. Mapping human autosomes: assignment of the MN locus to a specific segment in the long arm of chromosome no. 2.
    German J; Chaganti RS
    Science; 1973 Dec; 182(4118):1261-2. PubMed ID: 4752219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.
    Cohen MM; Davidson RG
    J Pediatr; 1971 Sep; 79(3):456-62. PubMed ID: 5567968
    [No Abstract]   [Full Text] [Related]  

  • 16. Chromosomal abnormalities in a girl with physical and mental maldevelopment.
    Subrt I; Hníková O
    Hum Hered; 1970; 20(3):252-9. PubMed ID: 5489883
    [No Abstract]   [Full Text] [Related]  

  • 17. Human chromosomal deficiency: the 4p--syndrome.
    Passarge E; Altrogge HC; Rüdiger RA
    Humangenetik; 1970 Aug; 10(1):51-7. PubMed ID: 5449950
    [No Abstract]   [Full Text] [Related]  

  • 18. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M; Niebuhr E
    Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
    [No Abstract]   [Full Text] [Related]  

  • 19. A retarded child with a 46XX,3p-q+ chromosome karyotype.
    Butler LJ; Hall ME; Wharton BA
    J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443
    [No Abstract]   [Full Text] [Related]  

  • 20. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.