Original Research
Published on 03 Mar 2022
MAP3K1 Variant Causes Hyperactivation of Wnt4/β-Catenin/FOXL2 Signaling Contributing to 46,XY Disorders/Differences of Sex Development
in Genetics of Common and Rare Diseases
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Original Research
Published on 03 Mar 2022
in Genetics of Common and Rare Diseases
Case Report
Published on 03 Mar 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 02 Mar 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 28 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 28 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 28 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 25 Feb 2022
in Genetics of Common and Rare Diseases
Editorial
Published on 25 Feb 2022
in Genetics of Common and Rare Diseases
Case Report
Published on 24 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 24 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 24 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 24 Feb 2022
in Genetics of Common and Rare Diseases
Case Report
Published on 23 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 23 Feb 2022
in Genetics of Common and Rare Diseases
Case Report
Published on 23 Feb 2022
in Genetics of Common and Rare Diseases
Original Research
Published on 22 Feb 2022
in Genetics of Common and Rare Diseases