Items where Author is "Stubbs, Matthew"
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Article
Chan, Melissa V
Hayman, Melissa A
Sivapalaratnam, Suthesh
Crescente, Marilena 
ORCID: https://orcid.org/0000-0003-3164-512X
Allan, Harriet E
Edin, Matthew L
Zeldin, Darryl C
et al.
ORCID: https://orcid.org/0000-0003-3164-512X
Allan, Harriet E
Edin, Matthew L
Zeldin, Darryl C
et al.
Chan, Melissa V, Hayman, Melissa A, Sivapalaratnam, Suthesh, Crescente, Marilena ORCID: https://orcid.org/0000-0003-3164-512X, Allan, Harriet E, Edin, Matthew L, Zeldin, Darryl C, Milne, Ginger L, Stephens, Jonathan, Greene, Daniel, Hanif, Moghees, O'Donnell, Valerie B, Dong, Liang, Malkowski, Michael G, Lentaigne, Claire, Wedderburn, Katherine, Stubbs, Matthew, Downes, Kate, Ouwehand, Willem H, Turro, Ernest, NIHR BioResource, Hart, Daniel P, Freson, Kathleen, Laffan, Michael A and Warner, Timothy D
(2020)
Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function.
Haematologic, 106 (5).
pp. 1423-1432.
ISSN 0390-6078
ORCID: https://orcid.org/0000-0003-3164-512X, Allan, Harriet E, Edin, Matthew L, Zeldin, Darryl C, Milne, Ginger L, Stephens, Jonathan, Greene, Daniel, Hanif, Moghees, O'Donnell, Valerie B, Dong, Liang, Malkowski, Michael G, Lentaigne, Claire, Wedderburn, Katherine, Stubbs, Matthew, Downes, Kate, Ouwehand, Willem H, Turro, Ernest, NIHR BioResource, Hart, Daniel P, Freson, Kathleen, Laffan, Michael A and Warner, Timothy D