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

138 related items for PubMed ID: 6371233

  • 1. A computerised data base for the diagnosis of rare dysmorphic syndromes.
    Winter RM, Baraitser M, Douglas JM.
    J Med Genet; 1984 Apr; 21(2):121-3. PubMed ID: 6371233
    [Abstract] [Full Text] [Related]

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

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

  • 4. SYNDROC: microcomputer based differential diagnosis of malformation patterns.
    Schorderet D, Aebischer P.
    Arch Dis Child; 1985 Mar; 60(3):248-51. PubMed ID: 3885868
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Microcomputer based differential diagnosis of dysmorphic syndromes.
    Veloso ML, Feijóo MJ.
    Ophthalmic Paediatr Genet; 1989 Mar; 10(1):47-50. PubMed ID: 2662096
    [Abstract] [Full Text] [Related]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A combinatorial method for grouping cases with multiple malformations.
    Winter RM, Clark RD, Ashley K, Gibbs G.
    J Med Genet; 1988 Feb; 25(2):118-21. PubMed ID: 3279212
    [Abstract] [Full Text] [Related]

  • 10. Diagnosing human malformation patterns with a microcomputer: evaluation of two different algorithms.
    Schorderet DF.
    Am J Med Genet; 1987 Oct; 28(2):337-44. PubMed ID: 3322003
    [Abstract] [Full Text] [Related]

  • 11. [Value of the Syndromselect microcomputer diagnostic program in the differential diagnosis of patients with multiple morphological abnormalities].
    Wilhelm O, Fehérvári I.
    Orv Hetil; 1988 Apr 17; 129(16):831-3. PubMed ID: 3290763
    [No Abstract] [Full Text] [Related]

  • 12. A chromosome supplement to the London Dysmorphology Database.
    Brandl J, Grimm T.
    J Med Genet; 1987 Aug 17; 24(8):497-8. PubMed ID: 3656373
    [Abstract] [Full Text] [Related]

  • 13. PC-based system for classifying dysmorphic syndromes in children.
    Wiener F, Annerén G.
    Comput Methods Programs Biomed; 1989 Feb 17; 28(2):111-7. PubMed ID: 2924554
    [Abstract] [Full Text] [Related]

  • 14. Computerized Dysmorphology Database Mackay (CDDM): preliminary report.
    Hsu CH, Lin SP, Huang FY.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994 Feb 17; 35(1):19-26. PubMed ID: 8178639
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. François syndrome. Early diagnosis and management.
    Walther JU, Konopizky B, Schimanek P.
    Ophthalmic Paediatr Genet; 1985 Aug 17; 6(1-2):303-6. PubMed ID: 4069589
    [No Abstract] [Full Text] [Related]

  • 20. Diagnosis in dysmorphology: clues from the skin.
    Smithson SF, Winter RM.
    Br J Dermatol; 2004 Nov 17; 151(5):953-60. PubMed ID: 15541072
    [Abstract] [Full Text] [Related]

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