Elsevier电子期刊(15)
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1.Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases
作者:Manu Jamwalp>ap>p> ; p>p>manujamwal25@gmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Anu Aggarwalp>ap>p> ; p>p>aggarwalanu2011@gmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Verinder Kumarp>ap>p> ; p>p>verinderkumar@gmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Prashant Sharmap>ap>p> ; p>p>prashant.sh@gmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Man Updesh Singh Sachdevap>ap>p> ; p>p>drmanupdeshpgi@yahoo.co.in" class="auth_mail" title="E-mail the corresponding authorp> ; Deepak Bansalp>bp>p> ; p>p>deepakbansaldr@gmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Pankaj Malhotrap>cp>p> ; p>p>malhotrapankaj@hotmail.com" class="auth_mail" title="E-mail the corresponding authorp> ; Reena Dasp>ap>p> ; p>p>das.reena@pgimer.edu.in" class="auth_mail" title="E-mail the corresponding authorp>p> ; p>p>reenadaspgi@hotmail.com" class="auth_mail" title="E-mail the corresponding authorp>
刊名:Clinica Chimica Acta
出版年:2016
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