Case Report
Published on 10 Aug 2023
Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene
in Genetics of Common and Rare Diseases
- 2,731 views
- 2 citations
Case Report
Published on 10 Aug 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 09 Aug 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 01 Aug 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 27 Jul 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 27 Jul 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 21 Jul 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 17 Jul 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 12 Jul 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 06 Jul 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 05 Jul 2023
in Genetics of Common and Rare Diseases
Review
Published on 27 Jun 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 27 Jun 2023
in Genetics of Common and Rare Diseases
Review
Published on 26 Jun 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 19 Jun 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 13 Jun 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 07 Jun 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 30 May 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 25 May 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 25 May 2023
in Genetics of Common and Rare Diseases
Review
Published on 22 May 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 19 May 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 19 May 2023
in Genetics of Common and Rare Diseases
Original Research
Published on 10 May 2023
in Genetics of Common and Rare Diseases
Case Report
Published on 05 May 2023
in Genetics of Common and Rare Diseases