Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hh, Boven"'
Publikováno v:
Europe PubMed Central
To assess the contribution of inherited antithrombin deficiency to mortality, we investigated the causes of death in 14 families with inherited antithrombin deficiency. Between 1830 and 1994, 86 of 266 family members who had a probability of 0.5 or m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::126a4faaf29be6f0f8a6588739b23692
https://pubmed.ncbi.nlm.nih.gov/9065992
https://pubmed.ncbi.nlm.nih.gov/9065992
Autor:
Hh, Boven, Rj, Olds, Sl, Thein, Ph, Reitsma, Da, Lane, Briët E, Jan P Vandenbroucke, Fr, Rosendaal
Publikováno v:
Europe PubMed Central
We studied the molecular basis and genetic heterogeneity of hereditary antithrombin (III) deficiency in nine Dutch families. Polymerase chain reaction (PCR) amplification and direct sequencing of all antithrombin gene exons and flanking intronic regi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::57f44f8dc4935b40ee9dbf5adf565e0f
https://pubmed.ncbi.nlm.nih.gov/7994035
https://pubmed.ncbi.nlm.nih.gov/7994035
Publikováno v:
Europe PubMed Central
To analyze inherited antithrombin deficiency as a risk factor for venous thromboembolism in various conditions with regard to the presence or absence of additional genetic or acquired risk factors, we compared 48 antithrombin-deficient individuals wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d2dfa0f546ec8c8f07538070af7fa741
http://europepmc.org/abstract/med/10515862
http://europepmc.org/abstract/med/10515862
