Recurrent nonimmune hydrops fetalis associated with carbohydrate-deficient glycoprotein syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005496920435/fullpdf
Reference3 articles.
1. Carbohydrate deficient glycoprotein (CDG) syndrome type 1;Jaeken;J Med Genet,1997
2. Hydrops fetalis: manifestation in lysosomal storage diseases including Farber disease;Kattner;Eur J Pediatr,1997
3. Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome);Matthijs;Nature Genetics,1997
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