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The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism
Download from www.ncbi.nlm.nih.govStructural and functional analysis of mutations in alkaptonuria
Download from academic.oup.comFamilial Syndromic Esophageal Atresia Maps to 2p23-p24
Download from www.ncbi.nlm.nih.govMolecular basis or factor H and FHL-1 deficiency in an Italian family
UploadAn integrated map of the human regulator of complement activation (RCA) gene cluster on 1q32
UploadA radiation hybrid map of complement factor H and factor H-related genes
UploadGenomic Cloning, Structure, Expression Pattern, and Chromosomal Location of the HumanSIX3Gene
Download from www.researchgate.netThe Human Homogentisate 1,2-Dioxygenase (HGO) Gene
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