HuGE Literature Finder
Records 1-3
Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects.
Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 63-5. Zahedpasha Yadollah, Ahmadpour Mousa, Niaki Haleh Akhavan, Alaee Ehs |
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
The Malaysian journal of pathology 2011 Dec 33 (2): 95-100. Azlin I, Wong F L, Ezham M, Hafiza A, Ainoon |
Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population.
Malaria journal 2009 Jul 8 (1): 1. Hue NT, Charlieu JP, Chau TT, Day NP, Farrrar JJ, Hien TT, Dunstan SJ |
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