Case Report
Published on 06 Oct 2022
Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay
in Genetics of Common and Rare Diseases

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Case Report
Published on 06 Oct 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 06 Oct 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 03 Oct 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 28 Sep 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 14 Sep 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 14 Sep 2022
in Genetics of Common and Rare Diseases

Brief Research Report
Published on 14 Sep 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 08 Sep 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 08 Sep 2022
in Genetics of Common and Rare Diseases

Mini Review
Published on 06 Sep 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 06 Sep 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 31 Aug 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 30 Aug 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 26 Aug 2022
in Genetics of Common and Rare Diseases

Case Report
Published on 25 Aug 2022
in Genetics of Common and Rare Diseases

Original Research
Published on 23 Aug 2022
in Genetics of Common and Rare Diseases
