Učitavanje...

Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region

Human chromosome 14q32.2 carries paternally expressed genes including DLK1 and RTL1, and maternally expressed genes including MEG3 and RTL1as, along with the germline-derived DLK1-MEG3 intergenic differentially methylated region (IG-DMR) and the postfertilization-derived MEG3-DMR. Consistent with th...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:J Hum Genet
Glavni autori: Ogata, Tsutomu, Kagami, Masayo
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2016
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4771937/
https://ncbi.nlm.nih.gov/pubmed/26377239
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.113
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!