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Journal Abstract Search

76 related items for PubMed ID: 938603

  • 1. Pseudogout: session II. Genetics of CPPD deposition: discussion.
    Arthritis Rheum; 1976; 19 Suppl 3():410-1. PubMed ID: 938603
    [No Abstract] [Full Text] [Related]

  • 2. [Hereditary chondrocalcinosis in a Swiss family].
    Gerster JC, Schmied PA.
    Schweiz Med Wochenschr; 1987 Mar 14; 117(11):402-5. PubMed ID: 3576151
    [Abstract] [Full Text] [Related]

  • 3. [Chromosome anomalies and genetics].
    Higurashi M, Matsui I, Naganuma M.
    Naika; 1969 Apr 14; 23(4):633-7. PubMed ID: 5800501
    [No Abstract] [Full Text] [Related]

  • 4. HL-A system in articular chondrocalcinosis.
    Nyulassy S, Stefanovic J, Sitaj S, Zitnan D.
    Arthritis Rheum; 1976 Apr 14; 19 Suppl 3():391-3. PubMed ID: 938601
    [No Abstract] [Full Text] [Related]

  • 5. [Hereditary chondrocalcinosis in Tunisia. Apropos of 3 families].
    Hamza M, Meddeb N, Bardin T, Hajri R, Mahmoudi B, Absia H, Sellami S.
    Rev Rhum Mal Osteoartic; 1991 Jun 14; 58(6):441-7. PubMed ID: 1896785
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary chondrocalcinosis in Switzerland: a new family].
    Gerster JC.
    Schweiz Med Wochenschr; 1990 Mar 03; 120(9):318. PubMed ID: 2315656
    [No Abstract] [Full Text] [Related]

  • 7. Public health and long-term genetic implications of intrauterine diagnosis and selective abortion.
    Motulsky AG, Fraser GR, Felsenstein J.
    Birth Defects Orig Artic Ser; 1971 Apr 03; 7(5):22-32. PubMed ID: 5120222
    [No Abstract] [Full Text] [Related]

  • 8. [Palmar ridge count. Heredity and clinical applications].
    Benigno V, Di Peri S, Boncori R, Como G, Distefano F.
    Minerva Pediatr; 1988 May 03; 40(5):259-64. PubMed ID: 3173277
    [No Abstract] [Full Text] [Related]

  • 9. [Current problems of clinical genetics].
    Davidenkova EF.
    Vestn Akad Med Nauk SSSR; 1976 May 03; (7):68-76. PubMed ID: 1027303
    [No Abstract] [Full Text] [Related]

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  • 12. A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies.
    Nielsen KB, Dyggve HV, Knudsen H, Olsen J.
    Dan Med Bull; 1983 Feb 03; 30(1):5-13. PubMed ID: 6831943
    [No Abstract] [Full Text] [Related]

  • 13. [Genetics and genetic diseases (V)].
    Xu WH.
    Zhonghua Hu Li Za Zhi; 1984 Oct 03; 19(5):305-9. PubMed ID: 6570667
    [No Abstract] [Full Text] [Related]

  • 14. The mutation rate in man.
    Edwards JH.
    Prog Med Genet; 1974 Oct 03; 10():1-16. PubMed ID: 4620173
    [No Abstract] [Full Text] [Related]

  • 15. Cancer genetics. II. Studies in humans. Problems in human studies.
    Lynch HT.
    Nebr Med J; 1973 Nov 03; 58(11):401-7. PubMed ID: 4585611
    [No Abstract] [Full Text] [Related]

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  • 20. [The type of inheritance of anhidrotic ectodermal dysplasia].
    Al'tshuler BA, Suvorova KN.
    Vestn Dermatol Venerol; 1984 Feb 03; (2):15-8. PubMed ID: 6720063
    [No Abstract] [Full Text] [Related]

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