Original Research
Published on 09 Feb 2023
Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi province
in Genetics of Common and Rare Diseases
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Original Research
Published on 09 Feb 2023
in Genetics of Common and Rare Diseases
Brief Research Report
Published on 09 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 08 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 06 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 03 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 02 Feb 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 02 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 01 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 01 Feb 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 01 Feb 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 30 Jan 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 27 Jan 2023
in Genetics of Common and Rare Diseases
Editorial
Published on 27 Jan 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 27 Jan 2023
in Genetics of Common and Rare Diseases
Editorial
Published on 26 Jan 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 26 Jan 2023
in Genetics of Common and Rare Diseases