Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Syndrome and G6PD[original query] |
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| 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 |
| 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 |
| 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 |
| Loss-of-function G6PD variant moderated high fat diet-induced obesity, adipocyte hypertrophy, and fatty liver in male rats. The Journal of biological chemistry 2024 6 107460. Shun Matsumura, Christina Signoretti, Samuel Fatehi, Bat Ider Tumenbayar, Catherine D'Addario, Erik Nimmer, Colin Thomas, Trisha Viswanathan, Alexandra Wolf, Victor Garcia, Petra Rocic, Yongho Bae, S M Shafiqul Alam, Sachin A Gup |
| Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais. BMC medical genomics 2024 1 17 (1): 9. Wanna Chetruengchai, Prasit Phowthongkum, Vorasuk Shotelers |
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