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  1. Article ; Online: A simple method for selecting urine samples that need culturing.

    Anad F

    Annals of Saudi Medicine, Vol 21, Iss -1, Pp 104-

    2001  Volume 5

    Keywords Medicine (General) ; R5-920 ; Medicine ; R ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2001-01-01T00:00:00Z
    Publisher King Faisal Specialist Hospital and Research Centre
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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  2. Article: A simple method for selecting urine samples that need culturing.

    Anad, F Y

    Annals of Saudi medicine

    2007  Volume 21, Issue 1-2, Page(s) 104–105

    Language English
    Publishing date 2007-01-28
    Publishing country Saudi Arabia
    Document type Journal Article
    ZDB-ID 639014-6
    ISSN 0975-4466 ; 0256-4947
    ISSN (online) 0975-4466
    ISSN 0256-4947
    DOI 10.5144/0256-4947.2001.104
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Alagille syndrome and deletion of 20p.

    Anad, F / Burn, J / Matthews, D / Cross, I / Davison, B C / Mueller, R / Sands, M / Lillington, D M / Eastham, E

    Journal of medical genetics

    1990  Volume 27, Issue 12, Page(s) 729–737

    Abstract: We add five cases of 20p deletion to the 10 cases already published. Four had craniofacial, vertebral, ocular, and cardiovascular features of Alagille syndrome, which adds weight to the assignment of this disorder to the short arm of chromosome 20. ... ...

    Abstract We add five cases of 20p deletion to the 10 cases already published. Four had craniofacial, vertebral, ocular, and cardiovascular features of Alagille syndrome, which adds weight to the assignment of this disorder to the short arm of chromosome 20. Included in our series is the first report of familial transmission of a 20p deletion.
    MeSH term(s) Abnormalities, Multiple/genetics ; Adolescent ; Adult ; Bone and Bones/abnormalities ; Child, Preschool ; Cholestasis/genetics ; Chromosome Banding ; Chromosome Deletion ; Chromosomes, Human, Pair 20 ; Eye Abnormalities/genetics ; Facial Bones/abnormalities ; Female ; Heart Defects, Congenital/genetics ; Humans ; Infant ; Kidney/abnormalities ; Male ; Skull/abnormalities ; Syndrome
    Language English
    Publishing date 1990-12
    Publishing country England
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 220881-7
    ISSN 1468-6244 ; 0022-2593
    ISSN (online) 1468-6244
    ISSN 0022-2593
    DOI 10.1136/jmg.27.12.729
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

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