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 *

144 related articles for article (PubMed ID: 5149537)

  • 1. A ring-4 chromosome in a patient with normal intelligence and short stature.
    Surana RB; Bailey JD; Conen PE
    J Med Genet; 1971 Dec; 8(4):517-21. PubMed ID: 5149537
    [No Abstract]   [Full Text] [Related]  

  • 2. Two human X-autosome translocations identified by autoradiography and fluorescence.
    Cohen MM; Lin CC; Sybert V; Orecchio EJ
    Am J Hum Genet; 1972 Sep; 24(5):583-97. PubMed ID: 5054227
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Evidence for X-X chromosome translocation in humans.
    Sinha AK; Nora JJ
    Ann Hum Genet; 1969 Oct; 33(2):117-24. PubMed ID: 5383978
    [No Abstract]   [Full Text] [Related]  

  • 5. Conenital hypothyroidism in association with a ring chromosome 18.
    Winter JS; Ahluwalia K; Ray M
    J Med Genet; 1972 Mar; 9(1):122-6. PubMed ID: 5025476
    [No Abstract]   [Full Text] [Related]  

  • 6. A partial D-trisomy-normal mosaic female.
    Webb GC; Garson M; Robson MK; Pitt DB
    J Med Genet; 1971 Dec; 8(4):522-7. PubMed ID: 5149538
    [No Abstract]   [Full Text] [Related]  

  • 7. X chromosome long arm deletion in a patient with Down's syndrome.
    Luthardt FW; Palmer CG
    J Med Genet; 1971 Sep; 8(3):387-91. PubMed ID: 4255466
    [No Abstract]   [Full Text] [Related]  

  • 8. Apparent deletion of X chromosome in a prepuberal girl.
    Steinberger E; Steinberger A; Smith KD; Perloff WH
    J Med Genet; 1966 Sep; 3(3):226-9. PubMed ID: 5971058
    [No Abstract]   [Full Text] [Related]  

  • 9. A case of 48,XXXX female with normal intelligence.
    Blackston RD; Chen AT
    J Med Genet; 1972 Jun; 9(2):230-2. PubMed ID: 5046634
    [No Abstract]   [Full Text] [Related]  

  • 10. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Weber FM; Sparkes RS; Muller H
    Cytogenetics; 1971; 10(6):404-12. PubMed ID: 5146417
    [No Abstract]   [Full Text] [Related]  

  • 11. Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
    Bocian M; Krmpotic E; Szego K; Rosenthal IM
    J Med Genet; 1971 Sep; 8(3):358-63. PubMed ID: 5097143
    [No Abstract]   [Full Text] [Related]  

  • 12. Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism.
    Cooke P; Black JA; Curtis DJ
    J Med Genet; 1972 Jun; 9(2):235-8. PubMed ID: 5046636
    [No Abstract]   [Full Text] [Related]  

  • 13. Isochromosomes arising from a human 'C'-autosome.
    Sinha AK; Nora JJ; Pathak S
    Hum Hered; 1971; 21(3):231-7. PubMed ID: 5136211
    [No Abstract]   [Full Text] [Related]  

  • 14. Human chromosome identification and the pattern of DNA replication in fibroblasts from an XXY male. A quantitative autoradiographic study of early and late synthesis.
    Ockey CH
    Cytogenetics; 1969; 8(4):272-95. PubMed ID: 4245462
    [No Abstract]   [Full Text] [Related]  

  • 15. Human chromosome identification and the pattern of DNA replication in fibroblasts from an XXY male. A quantitative autoradiographic study of early and late synthesis.
    Ockey CH
    Cytogenetics; 1969; 8(5):272-95. PubMed ID: 4242064
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes.
    Polani PE; Angell R; Giannelli F; De la Chapelle A; Race RR; Sanger R
    Nature; 1970 Aug; 227(5258):613-6. PubMed ID: 5429293
    [No Abstract]   [Full Text] [Related]  

  • 18. Multiple congenital defects associated with an abnormal unclassifiable karyotype.
    Surana RB; Hunt TM; Conen PE
    J Med Genet; 1972 Jun; 9(2):247-9. PubMed ID: 5046638
    [No Abstract]   [Full Text] [Related]  

  • 19. Sex chromatin survey among mentally retarded children in Japan.
    Yanagisawa S; Shuto T
    J Ment Defic Res; 1970 Sep; 14(3):254-62. PubMed ID: 5518410
    [No Abstract]   [Full Text] [Related]  

  • 20. Autoradiographic re-appraisal of an XXXxY male as a probable XXXXY with a 4-11 translocation.
    Ockey CH; De la Chapelle A
    Cytogenetics; 1967; 6(3):178-92. PubMed ID: 6040472
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.