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Molecular screening and prenatal diagnosis for finnish congenital nephrosis in low risk pregnancies in Finland

✍ Scribed by J. Kallinen; A. Mannermaa; S. Heinonen; P. Kirkinen; M. Ryynänen


Book ID
117125468
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
173 KB
Volume
70
Category
Article
ISSN
0020-7292

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📜 SIMILAR VOLUMES


PRENATAL SCREENING FOR CONGENITAL NEPHRO
✍ SEPPO HEINONEN; MARKKU RYYNÄNEN; PERTTI KIRKINEN; ILKKA PENTTILÄ; KARI SYRJÄNEN; 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 545 KB

Congenital nephrosis of the Finnish type (CNF) is inherited as an autosomal recessive trait which maps to the long arm of chromosome 19. The disease causes massive proteinuria, and renal transplantation in early neonatal life is the only effective treatment. Prenatal diagnosis, usually in high-risk