Pages that link to "Q34084829"
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The following pages link to Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. (Q34084829):
Displaying 4 items.
- Compromised fertility disrupts Peg1 but not Snrpn and Peg3 imprinted methylation acquisition in mouse oocytes. (Q36088644) (← links)
- High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos (Q36340375) (← links)
- A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes (Q36634304) (← links)
- Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture. (Q50350055) (← links)