Search Results - "RAUDSEPP, Heli"

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    Autosomal recessive congenital ichthyosis in Sweden and Estonia: Clinical, genetic and ultrastructural findings in eighty-three patients

    Autosomal recessive congenital ichthyosis in Sweden and Estonia: Clinical, genetic and ultrastructural findings in eighty-three patients by GANEMO, Agneta, PIGG, Maritta, VIRTANEN, Marie, KUKK, Terje, RAUDSEPP, Heli, ROSSMAN-RINGDAHL, Ingrid, WESTERMARK, Per, NIEMI, Kirsti-Maria, DAHL, Niklas, VAHLQUIST, Anders

    Published in Acta dermato-venereologica (2003)
    “…Congenital (non-bullous) ichthyosis is a rare group of keratinizing disorders which can be tentatively subclassified based on clinical criteria, analysis of…”
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    Autosomal recessive congenital ichthyosis in Sweden and Estonia: clinical, genetic and ultrastructural findings in eithty-three patients

    Autosomal recessive congenital ichthyosis in Sweden and Estonia: clinical, genetic and ultrastructural findings in eithty-three patients by Gånemo, Agneta, Pigg, Maritta, Virtanen, Marie, Kukk, Terje, Raudsepp, Heli, Rossman-Ringdahl, Ingrid, Westermark, Per, Niemi, Kirsti-Maria, Dahl, Niklas, Vahlquist, Anders

    Published in Acta dermato-venereologica (2003)
    “…Congenital (non-bullous) ichthyosis is a rare group of keratinizing disorders which can be tentatively subclassified based on clinical criteria, analysis of…”
    Get full text
    Journal Article
    Save to List
    Saved in:

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