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Defining the phenotype in an autosomal recessive cutis laxa …
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
Article, Chapter
Authors: E. Morava
Publication: European Journal of Human Genetics, Volume:16, Issue:1, Page(s):28-35
Published: 2008
ISSN: 1018-4813
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View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,Springer Complete Journals Opens in new Window
Journal:  European Journal of Human Genetics Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1993-01-01~present; volume:1~present;issue:1~present
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