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Q50422325-BC9E3F28-45C6-41E0-B24C-A328B6895C82
Q50422325-BC9E3F28-45C6-41E0-B24C-A328B6895C82
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50422325-BC9E3F28-45C6-41E0-B24C-A328B6895C82
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.
P2860
Q50422325-BC9E3F28-45C6-41E0-B24C-A328B6895C82
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50422325-BC9E3F28-45C6-41E0-B24C-A328B6895C82
rank
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type
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Statement
wasDerivedFrom
a3f13d4cc92c50834ca671698b346e41780a6675
P2860
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.