NDLTD Global ETD Search
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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.

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Showing 1 to 2 of 2 (0.06 seconds)

Spelling suggestions: "subject:"zellweger syndrome"" "subject:"hellwegeri syndrome""

1

Étude clinique, génétique et épidémiologique du syndrome de Zellweger et de la cystinose au Saguenay-Lac-St-Jean /

Brassard, Joëlle, January 1993 (has links)
Mémoire (M.Med.Exp.)-- Université du Québec à Chicoutimi, 1993. / Document électronique également accessible en format PDF. CaQCU
Zellweger, Syndrome de Cystinose
2

Analyse des PEX1-Gens bei Patienten mit Zellweger-Syndrom: Identifikation einer neuen Deletion und Untersuchung von Polymorphismen in der 5'-untranslatierten Region / Analysis of the PEX1 gene of patients with Zellweger syndrome: Identification of a novel deletion and characterization of polymorphisms in the 5' untranslated region

Rabenau, Jana 19 July 2011 (has links)
No description available.
610 Medizin, Gesundheit
Medicine
Peroxisomen
Zellweger-Syndrom
Peroxisomenbiogenesedefekt
PEX1
5 UTR-Polymorphismen
SNP
peroxisome
Zellweger syndrome
peroxisome biogenesis disorder
PEX1
5 UTR polymorphisms
SNP
44.67
MED 461 Pädiatrie

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