Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene-Reference-Cited by-同舟云学术

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Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene

Published:1998-02-03 Issue:3 Volume:95 Page:1102-1107
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Miyoshi N.,Kuroiwa Y.,Kohda T.,Shitara H.,Yonekawa H.,Kawabe T.,Hasegawa H.,Barton S. C.,Surani M. A.,Kaneko-Ishino T.,Ishino F.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference52 articles.

1. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

2. Completion of mouse embryogenesis requires both the maternal and paternal genomes

3. Differential activity of maternally and paternally derived chromosome regions in mice

4. A new genetic concept: Uniparental disomy and its potential effect, isodisomy

5. Genomic imprinting and genetic disorders in man

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4. Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic Review;Current Pediatric Reviews;2023-05

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