Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Katie L. Miles"'
Publikováno v:
Legal and Criminological Psychology. 12:217-232
Purpose. This study explored the effectiveness of the Gudjonsson Suggestibility Scale for Children, version 2 in predicting the tendency of older school-aged children (with and without intellectual disabilities) to generate errors in an independent s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2d1fa8f5afd7b4944fdd5275dd6c42e
https://doi.org/10.1348/135532506x116750
https://doi.org/10.1348/135532506x116750
Publikováno v:
Applied Cognitive Psychology. 18:1021-1036
This study compared the effectiveness of two standardized suggestibility paradigms in predicting preschoolers' tendency to report an independent, non-experienced event. Ninety-three children, aged 47 to 64 months, were given a description of a non-ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae7715eab5b5cc237e7fe7e0bb6f7c7a
https://doi.org/10.1002/acp.1074
https://doi.org/10.1002/acp.1074
Publikováno v:
British Journal of Haematology. 113:694-698
Polymerase chain reaction protocols were designed specifically to amplify regions of the alpha globin complex that contain the nine common polymorphic haplotyping sites. These reactions provided a quicker and more sensitive approach to determining al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::490f592d8578c8a482c30bf563b38b0f
https://doi.org/10.1046/j.1365-2141.2001.02823.x
https://doi.org/10.1046/j.1365-2141.2001.02823.x
Autor:
Katie L Miles, Jennifer J. Pointon, Michael Steiner, Alison T. Merryweather-Clarke, Tran Tinh Hien, Vip Viprakasit, Karen Livesey, Sean O’Riordan, Kathryn J. H. Robson
Publikováno v:
Blood cells, moleculesdiseases. 30(3)
Hereditary hemochromatosis (HH) is an autosomal recessive disease caused by mutations in the HFE gene that mainly affects populations of European descent. Recently a novel mutation (IVS5+1 G→A) has been described in a Vietnamese patient with HH tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad5f7feaf53745fd72c8e237669e6f68
https://pubmed.ncbi.nlm.nih.gov/12737949
https://pubmed.ncbi.nlm.nih.gov/12737949
Autor:
Aranya Wiriyasateinkul, Vichai Laosombat, Vip Viprakasit, Benjamas Sattayasevana, Katie L. Miles
Publikováno v:
Hemoglobin. 26(3)
We report a Thai family in which five members are Hb G-Makassar heterozygotes and one member is, in addition, a heterozygote for beta0-thalassemia (IVS-I-1, G--T). We confirm that the previously presumed mutation at codon 6 of the beta-globin gene is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a787b8b1423a7ccfb859b6b9d5997e
https://pubmed.ncbi.nlm.nih.gov/12403489
https://pubmed.ncbi.nlm.nih.gov/12403489