Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype

Overview of attention for article published in Frontiers in Genetics, October 2021

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New Research: Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype: Alport syndrome with intellectual disability (ATS-ID, AMME complex; OMIM #300194) is an X-linked… https://t.co/5rJ

29 Oct 2021

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