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 *

117 related articles for article (PubMed ID: 14324864)

  • 1. GENETIC IMPLICATIONS OF HETEROPYKNOSIS OF THE X CHROMOSOME.
    THOMPSON MW
    Can J Genet Cytol; 1965 Jun; 7():202-13. PubMed ID: 14324864
    [No Abstract]   [Full Text] [Related]  

  • 2. GENES ON THE X CHROMOSOME.
    SANGER R
    Can J Genet Cytol; 1965 Jun; 7():179-88. PubMed ID: 14324862
    [No Abstract]   [Full Text] [Related]  

  • 3. A REVIEW OF OCULAR ABNORMALITIES ASSOCIATED WITH THE X CHROMOSOME.
    SPIVEY BE
    Surv Ophthalmol; 1965 Jun; 10():223-31. PubMed ID: 14320393
    [No Abstract]   [Full Text] [Related]  

  • 4. On the X chromosome of man.
    MCKUSICK VA
    Q Rev Biol; 1962 Jun; 37():69-175. PubMed ID: 13932119
    [No Abstract]   [Full Text] [Related]  

  • 5. [DISCUSSION OF THE PATERNAL ORIGIN OF THE X CHROMOSOME FROM A TURNER SYNDROME, XO, PROTANOPE AND XG (A-)].
    TURPIN R; LEJEUNE J; SALMON C
    C R Hebd Seances Acad Sci; 1965 Jan; 260():369-72. PubMed ID: 14308221
    [No Abstract]   [Full Text] [Related]  

  • 6. XG-A INVESTIGATIONS OF THE FAMILY OF A CHILD WITH A RING X CHROMOSOME.
    NIJENHUIS LE; GEMSER-RUNIA J
    Nature; 1964 Nov; 204():792-3. PubMed ID: 14235684
    [No Abstract]   [Full Text] [Related]  

  • 7. ANTIHEMOPHILIC GLOBULIN DEFICIENCY IN A CHROMOSOMAL FEMALE.
    LUSHERJMSTAUB RT; BELOTE JH
    Am J Dis Child; 1964 Sep; 108():309-14. PubMed ID: 14168070
    [No Abstract]   [Full Text] [Related]  

  • 8. "Genetic for medical practitioners".
    Ambani LM
    Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087
    [No Abstract]   [Full Text] [Related]  

  • 9. The anatomy of the human genome.
    McKusick VA
    Am J Med; 1980 Aug; 69(2):267-76. PubMed ID: 6931483
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The human genome--chromosome X. Focus on Xq28].
    Sedlácek Z
    Cas Lek Cesk; 1995 Dec; 134(23):760-6. PubMed ID: 8599818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Laboratory contributions to human cytogenetics.
    Teplitz RL
    JAMA; 1976 Jul; 236(4):376-8. PubMed ID: 947053
    [No Abstract]   [Full Text] [Related]  

  • 12. An ABC of medical genetics. II. Chromosomes and chromosome mutations.
    Carter CO
    Lancet; 1969 May; 1(7604):1041-5. PubMed ID: 4181267
    [No Abstract]   [Full Text] [Related]  

  • 13. [Klinefelter's syndrome and hypospadias. Presence of 2 X chromosomes. Rupture of Y chromosome and translocation of its fragments].
    LAMY M; de GROUCHY ; FREZAL J; JOSSO N; FEINTUCH G
    C R Hebd Seances Acad Sci; 1962 Jul; 255():581-3. PubMed ID: 14461880
    [No Abstract]   [Full Text] [Related]  

  • 14. Human gene mapping, genetic linkage, and clinical applications.
    Ann Intern Med; 1980 Sep; 93(3):469-79. PubMed ID: 6159813
    [TBL] [Abstract][Full Text] [Related]  

  • 15. IDENTIFICATION OF THE ORIGIN OF THE X CHROMOSOME(S) IN SEX CHROMOSOME ANEUPLOIDY.
    RACE RR
    Can J Genet Cytol; 1965 Jun; 7():214-22. PubMed ID: 14324865
    [No Abstract]   [Full Text] [Related]  

  • 16. SIZE VARIATION AND ORIENTATION OF THE HUMAN Y CHROMOSOME.
    GRIPENBERG U
    Chromosoma; 1964 Dec; 15():618-29. PubMed ID: 14333154
    [No Abstract]   [Full Text] [Related]  

  • 17. [Human chromosome aberrations].
    LEJEUNE J
    Brux Med; 1962 Jan; 42():107-22. PubMed ID: 14463930
    [No Abstract]   [Full Text] [Related]  

  • 18. [RECENT ASPECTS OF HUMAN GENETICS].
    HARVALD B
    Manedsskr Prakt Laegegern; 1964 Oct; 42():427-42. PubMed ID: 14239044
    [No Abstract]   [Full Text] [Related]  

  • 19. [TAPETO-RETINAL DEGENERATION OF THE X CHROMOSOME TYPE IN THE NETHERLANDS].
    SCHAPPERT-KIMMIJSER J
    Bull Mem Soc Fr Ophtalmol; 1963; 76():122-9. PubMed ID: 14174213
    [No Abstract]   [Full Text] [Related]  

  • 20. Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.
    Willard HF; Waye JS; Skolnick MH; Schwartz CE; Powers VE; England SB
    Proc Natl Acad Sci U S A; 1986 Aug; 83(15):5611-5. PubMed ID: 3016709
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.