Title |
Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome |
|---|---|
Involved |
Carla Eßinger (Verfasser)
Stephanie Karch (Verfasser) Ute Moog (Verfasser) György Fekete (Verfasser)
Anna Lengyel (Verfasser)
Eva Pinti (Verfasser) Thomas Eggermann (Verfasser) Matthias Begemann (Verfasser) SpringerLink (Online service) (Sonstige) |
Published in |
Clinical epigenetics 12, 1, 11.5.2020, date:12.2020, Seite 1-7 |
Published |
2020 |
Language |
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Country |
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Topic |
|
Subject |
Human Genetics. |
DDC notation |
|
Persistent identifier |
urn:nbn:de:101:1-2020071707283530001598 (URN) |
Record ID |
1213985226 |
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