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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

128 related items for PubMed ID: 5137684

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH, Finley SC, Monsky D.
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
    [No Abstract] [Full Text] [Related]

  • 9. The 4p-syndrome, with a report of two new cases.
    Fryns JP, Eggermont E, Verresen H, Van den Berghe H.
    Humangenetik; 1973 Sep; 19(1):99-109. PubMed ID: 4725911
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Trisomy 13-15.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):44-9. PubMed ID: 4302761
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19).
    Pallister PD, Patau K, Inhorn SL, Opitz JM.
    Clin Genet; 1974 Jan; 5(3):188-95. PubMed ID: 4209591
    [No Abstract] [Full Text] [Related]

  • 15. Trisomy 18.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
    [No Abstract] [Full Text] [Related]

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

  • 17. Interstitial deletion of the short arm of chromosome 4.
    Ray M, Evans J, Rockman-Greenberg C, Wickstrom D.
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [Abstract] [Full Text] [Related]

  • 18. Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.
    Hamers AJ, van Kempen C.
    J Med Genet; 1977 Dec; 14(6):451-5. PubMed ID: 604497
    [Abstract] [Full Text] [Related]

  • 19. The trisomy 8 syndrome: report of two further cases.
    Jacobsen P, Mikkelsen M, Rosleff F.
    Ann Genet; 1974 Jun; 17(2):87-94. PubMed ID: 4547945
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.