Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
(Q24308083)
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Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
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2027-32
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12
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5
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+1996-12-00T00:00:00Z
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"Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway" (language: en)
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K W Brown
A J Villar
W Bickmore
J Clayton-Smith
D Catchpoole
E R Maher
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