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dc.contributor.authorBlanchet-Bardon, C.fr_FR
dc.date.accessioned2013-02-18T16:18:02Z
dc.date.available2013-02-18T16:18:02Z
dc.date.issued1993fr_FR
dc.identifier.citationBlanchet-Bardon, C., Le diagnostic anténatal des génodermatoses, Med Sci (Paris), 1993, Vol. 9, N° 4; p.396-402fr_FR
dc.identifier.issn1958-5381fr_FR
dc.identifier.urihttp://hdl.handle.net/10608/2932
dc.description.abstractThe rapid development of techniques available for fetal examination and tissue sampling, coupled with novel methods for enzymological, cytogenetic and DNA analysis has enabled the intrauterine detection of fetal skin disorders to become an integral part of the management of several genetic skin diseases. The relevance of new prenatal diagnostic methods to genetic diseases with major cutaneous manifestations is still largely limited to the detection of structural abnormalities in fetal skin biopsies (epidermolysis bullosa, keratinization disorders, pigmentation disorders). But the enormous advances in molecular biology of the epidermolysis bullosa group and the epidermolytic hyperkeratosis will soon allow identification of affected fetuses and possibly carriers.fr
dc.language.isofrfr_FR
dc.publisherJohn Libbey Eurotext, Montrougefr_FR
dc.rightsArticle en libre accèsfr
dc.rightsMédecine/Sciences - Inserm - SRMSfr
dc.sourceM/S. Médecine sciences [revue papier, ISSN : 0767-0974], 1993, Vol. 9, N° 4; p.396-402fr_FR
dc.titleLe diagnostic anténatal des génodermatosesfr
dc.typeArticlefr_FR
dc.identifier.doi10.4267/10608/2932


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