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Springer Nature1
Journal
Human Genetics1
Publication Year
19971
Edwin Verlind results 1 · Newest (Page 1/1, per page 25)
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Author: Edwin Verlind ×Clear All Filters
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Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosaNARA Subscribed
Human Genetics · 1997 · Vol. 100 · Issue 2 · Springer
H. Scheffer; Rein P. Stulp; Edwin Verlind; M. van der Meulen; Leena Bruckner-Tuderman; Tobias Gedde-Dahl Jr.; G. J. te Meerman; Arnoud Sonnenberg; Charles H. C. M. Buys; Marcel F. Jonkman
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