Identification of an imprinted gene, Meg3 /Gtl2 and its human homologue MEG3 , first mapped on mouse distal chromosome 12 and human chromosome 14q-Reference-Cited by-同舟云学术

Identification of an imprinted gene, Meg3 /Gtl2 and its human homologue MEG3 , first mapped on mouse distal chromosome 12 and human chromosome 14q

Published:2000-03 Issue:3 Volume:5 Page:211-220
ISSN:1356-9597
Container-title:Genes to Cells
language:en
Short-container-title:Genes to Cells

Author:

Miyoshi Naoki,Wagatsuma Hirotaka,Wakana Shigeharu,Shiroishi Toshihiko,Nomura Masashi,Aisaka Kohzoh,Kohda Takashi,Surani M. Azim,Kaneko-Ishino Tomoko,Ishino Fumitoshi

Publisher

Wiley

Subject

Cell Biology,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2443.2000.00320.x/fullpdf

Reference37 articles.

1. 2C.V. Beechey, and B.M. Cattanach (1997 ).Mouse Genome95 , 161 .

2. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

3. Paternal uniparental disomy for chromosome 14: A case report and review

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