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Daniel J Hampshire

Showing results (1-10 of 20) with videos related to

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British Journal of Haematology|April 12, 2023
Factor VII deficiency: A cause of (or risk factor for) bleeding?Daniel J Hampshire
Haematologica|June 3, 2011
The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlookedDaniel J Hampshire, Anne C Goodeve
Seminars in Thrombosis and Hemostasis|November 22, 2011
The international society on thrombosis and haematosis von Willebrand disease database: an updateDaniel J Hampshire, Anne C Goodeve
Annals of Hematology|June 19, 2013
p.P2063S: a neutral VWF variant masquerading as a mutationDaniel J Hampshire, Anne C Goodeve
Seminars in Thrombosis and Hemostasis|August 6, 2019
A Bioinformatics Toolkit: In Silico Tools and Online Resources for Investigating Genetic VariationSimon J Webster, Maryam A Aldossary, Daniel J Hampshire
European Journal of Human Genetics : EJHG|February 24, 2006
MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34Daniel J Hampshire, Mohammed Ayub, Kelly Springell, et al.
Human Mutation|April 26, 2020
The EAHAD blood coagulation factor VII variant databaseMuriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2020
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchersJohn H McVey, Pavithra M Rallapalli, Geoffrey Kemball-Cook, et al.
Haematologica|September 21, 2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohortDaniel J Hampshire, George J Burghel, Jenny Goudemand, et al.
Nature Genetics|October 2, 2002
ASPM is a major determinant of cerebral cortical sizeJacquelyn Bond, Emma Roberts, Ganesh H Mochida, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
British Journal of Haematology|April 12, 2023
Factor VII deficiency: A cause of (or risk factor for) bleeding?Daniel J Hampshire
Haematologica|June 3, 2011
The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlookedDaniel J Hampshire, Anne C Goodeve
Seminars in Thrombosis and Hemostasis|November 22, 2011
The international society on thrombosis and haematosis von Willebrand disease database: an updateDaniel J Hampshire, Anne C Goodeve
Annals of Hematology|June 19, 2013
p.P2063S: a neutral VWF variant masquerading as a mutationDaniel J Hampshire, Anne C Goodeve
Seminars in Thrombosis and Hemostasis|August 6, 2019
A Bioinformatics Toolkit: In Silico Tools and Online Resources for Investigating Genetic VariationSimon J Webster, Maryam A Aldossary, Daniel J Hampshire
European Journal of Human Genetics : EJHG|February 24, 2006
MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34Daniel J Hampshire, Mohammed Ayub, Kelly Springell, et al.
Human Mutation|April 26, 2020
The EAHAD blood coagulation factor VII variant databaseMuriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2020
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchersJohn H McVey, Pavithra M Rallapalli, Geoffrey Kemball-Cook, et al.
Haematologica|September 21, 2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohortDaniel J Hampshire, George J Burghel, Jenny Goudemand, et al.
Nature Genetics|October 2, 2002
ASPM is a major determinant of cerebral cortical sizeJacquelyn Bond, Emma Roberts, Ganesh H Mochida, et al.
Pageof 2