A de novo 1p35.2 microdeletion...

Congenital Anomalies 2018 / 12

A de novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome

Imaizumi, Taichi, Mogami, Yukiko, Okamoto, Nobuhiko, Yamamoto‐Shimojima, Keiko, Yamamoto, Toshiyuki
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Language:
english
Journal:
Congenital Anomalies
DOI:
10.1111/cga.12322
Date:
December, 2018
File:
PDF, 723 KB
english, 2018
Conversion to is in progress
Conversion to is failed