20th World Congress of Dermatology
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CC1153
Wild phenotypic spectrum of TP63 mutations
IC1501
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema: a novel entity ascribed to mutation of the NEMO gene
IC1576
Impairing in NF-kB signaling is a common cause of incontinentia pigmenti and anhidrotic ectodermal dysplasia
IC1582
Homozygosity mapping of a locus for a novel form of syndromic ichthyosis to chromosome 3Q27
P0765
Trichothiodystrophy: unusual phenotypes


1st TO 5th JULY 2002
PARIS



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Foreword

Oral communications and co-opted speakers abstracts

Poster abstracts

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