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Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 09, Pp 03-05 (2023)
Wolf-Hirschhorn Syndrome (WHS), also known as Chromosome 4 deletion syndrome, is a rare hereditary disease with a prevalence of 1 in 50,000. It occurs due to the microdeletion of the short arm of chromosome 4, specifically the 4p16.3 domain. Patient
Externí odkaz:
https://doaj.org/article/aa45c77f6e064e37a6dc34a2a113f823