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Beckwith-Wiedemann syndrome due to imprinting defect of 11p15

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Name:
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
ORPHAcode:
231117
XREF(s):
Orphanet
ICD-10
Analyte(s):
H19
KCNQ1OT1
IGF2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14