Published in
Wiley, Congenital Anomalies, 6(59), p. 193-194, 2019
DOI: 10.1111/cga.12322
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De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome
Journal article published in 2019 by
Taichi Imaizumi,
Yukiko Mogami,
Nobuhiko Okamoto 
,
Keiko Yamamoto‐Shimojima,
Toshiyuki Yamamoto
,
Keiko Yamamoto‐Shimojima,
Toshiyuki Yamamoto
This paper was not found in any repository, but could be made available legally by the author.
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