Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Richard T. Wensley"'
Autor:
David Stuart Millar, Richard T. Wensley, Norma B. de Bosch, David Neil Cooper, Adrian Minford, Bent N. Johansen, Sam Schulman, Argimiro Torres, Vijay V. Kakkar, Paula H. B. Bolton-Maggs, Erik Berntorp
Publikováno v:
Human Genetics. 106:646-653
Severe protein C deficiency is a rare, early onset, venous thrombotic condition that is inherited as an autosomal recessive trait. The protein C (PROC) genes of nine unrelated individuals with severe protein C deficiency were sequenced yielding a tot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eacf896d721d57a37ad8e2830a2a8d7f
https://doi.org/10.1007/s004390000315
https://doi.org/10.1007/s004390000315
Publikováno v:
Human genetics. 89(2)
We have used the polymerase chain reaction to amplify two variable number of tandem repeats (VNTRs) within a region of repetitive DNA located in intron 40 of the von Willebrand factor (vWf) gene. Heterozygosity for VNTR I was observed in 30 out of 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bebd3955376f378ae51c4bc15576f659
https://pubmed.ncbi.nlm.nih.gov/1587530
https://pubmed.ncbi.nlm.nih.gov/1587530