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A Familial Case of Overgrowth Syndrome Caused by a 9q22.3 Microdeletion in a Mother and Daughter.

Hikari Yamada,Masaru Shimura,Hidekuni Takahashi,Shonosuke Nara,Yasuyuki Morishima,Soken Go,Toshiyuki Miyashita,Hironao Numabe,Hisashi Kawashima

European Journal of Medical Genetics（2020）

Cited 4|Views23
Key words
9q22.3 microdeletion,Gorlin syndrome,PTCH1,Overgrowth,miRNA,Let-7
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