Detection of the Finnish-Type Congenital Nephrotic Syndrome...

Clinical Chemistry 2000 / 06 Vol. 46; Iss. 6

Detection of the Finnish-Type Congenital Nephrotic Syndrome by Restriction Fragment Length Polymorphism and Dual-Color Oligonucleotide Ligation Assays

Romppanen, Eeva-Liisa, Mononen, Ilkka
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Volume:
46
Journal:
Clinical Chemistry
DOI:
10.1093/clinchem/46.6.811
Date:
June, 2000
File:
PDF, 252 KB
2000
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