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18p
18p- is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 40,000 births. ==Nomenclature==
The preferred terminology for this condition is 18p-. In the past, it has been referred to as partial monosomy 18p and, rarely, as “de Grouchy syndrome, type 1".
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「18p」の詳細全文を読む
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