Case Report: A Case Report and Literature Review of 3p Deletion Syndrome
https://www.frontiersin.org/articles/10.3389/fped.2021.618059/full
WEBFeb 10, 2021 · 3p deletion syndrome is a rare autosomal and contiguous genomic disorder characterized by the following: intellectual disability; motor developmental delay; unusual facial features (microcephaly, micrognathia, ptosis, long philtrum, low and deformed ears, polydactyly deformity); hypotonia; and other rarer symptoms, including congenital heart …
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