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/vufind/Search/Results?lookfor=%22Hampshire%2C+Daniel+J%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Hampshire%2C+Daniel+J%22&type=Person&sort=year
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PubPharm (33)
1
Factor VII deficiency : A cause of (or risk factor for) bleeding?
enthalten in:
British journal of haematology
| 2023
von
Hampshire, D.
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2
Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms
enthalten in:
Blood advances
| 2020
von
Cartwright, A.
|
Webster, S.
|
de Jong, A.
| +11
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3
The EAHAD blood coagulation factor VII variant database
enthalten in:
Human mutation
| 2020
von
Giansily-Blaizot, M.
|
Rallapalli, P.
|
Perkins, S.
| +5
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4
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases : Important resources for haemostasis clinicians and researchers
enthalten in:
Haemophilia : the official journal of the World Federation of Hemophilia
| 2020
von
McVey, J.
|
Rallapalli, P.
|
Kemball-Cook, G.
| +5
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5
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases : Important resources for haemostasis clinicians and researchers
enthalten in:
Haemophilia
| 2020
von
McVey, J.
|
Rallapalli, P.
|
Kemball‐Cook, G.
| +5
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6
A Bioinformatics Toolkit : In Silico Tools and Online Resources for Investigating Genetic Variation
enthalten in:
Seminars in thrombosis and hemostasis
| 2019
von
Webster, S.
|
Aldossary, M.
|
Hampshire, D.
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7
The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance
enthalten in:
Blood advances
| 2018
von
Mufti, A.
|
Ogiwara, K.
|
Swystun, L.
| +10
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8
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
enthalten in:
Blood
| 2016
von
Simeoni, I.
|
Stephens, J.
|
Hu, F.
| +76
CommentIn: Blood. 2016 Jun 9;127(23 ):2781-2. - PMID 27282940
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9
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
enthalten in:
Blood
| 2016
von
Simeoni, I.
|
Stephens, J.
|
Hu, F.
| +76
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10
p.P2063S : a neutral VWF variant masquerading as a mutation
enthalten in:
Annals of hematology
| 2014
von
Hampshire, D.
|
Goodeve, A.
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2
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