Items where Author is "Hanif, Moghees"
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            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
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
  
  
