Showing results 2 to 4 of 4
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Title | Author(s) | Issue Date | |
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2018 | |||
De novo mutations associated with sporadic cases of Caudal regresion syndrome Proceeding/Conference:European Journal of Human Genetics | 2014 | ||
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population Journal:BioMed Research International | 2018 |