Evgeny Vasilyev
0000-0003-1107-362X
3 papers found
Refreshing results…
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 gene in child from Russia
Familial case of late diagnosis of Persistence of Müllerian derivatives syndrome type 1
Genotype-based personalized correction of glycemic control in patients with MODY due to mutations in GCK, HNF1A AND HNF4A genes
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