Congenital von Willebrand's disease and clinical hypothyroidismSyed Adeel Hassan, Philip Kuriakose, Waqas Qureshi et al.|Haemophilia|2012Cited by 5
Hemolytic anemia with mutations SPTA1 c.6531-12C>T and SLC4A1 Pro868LeuVidhya Nair, Vijayalakshmi Donthireddy, Diego Cabrera-Fernandez|Unknown|2019Cited by 0