Art
J-GLOBAL ID:200902158440062126   Reference number:00A0596134

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.

初期ヒト及びマウスはいにおけるSNRPNエクソン1の新たに生じた欠失は父性から母性へのインプリントスイッチを生じる
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Material:
Volume: 25  Issue:Page: 74-78  Publication year: May. 10, 2000 
JST Material Number: W0430A  ISSN: 1061-4036  Document type: Article
Article type: 短報  Country of issue: United States (USA)  Language: ENGLISH (EN)
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Congenital diseases,deformities in general.  ,  Mental disorders  ,  Molecular genetics in general 

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