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Journal of Pediatric Surgery|July 1, 1996
No evidence of WT1 gene mutations in children with congenital diaphragmatic herniaA Nordenskjöld, M Tapper-Persson, M Anvret
Human Genetics|May 1, 1992
Genetic and blood coagulation characterization of "Swedish" families with von Willebrand's disease types I and III: new aspects of heredityM Anvret, M Blombäck, M Lindstedt, et al.
Urological Research|March 26, 1999
Screening for mutations in candidate genes for hypospadiasA Nordenskjöld, E Friedman, M Tapper-Persson, et al.
Human Genetics|August 1, 1994
Geographical distribution of haplotypes in Swedish families with Huntington's diseaseE Almqvist, S Andrew, J Theilmann, et al.
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