Ryuji Fukuzawa

Years Active: 2017-2018
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Hirohito Shima, Mie Hayashi, Takashi Tachibana, Makoto Oshiro, Naoko Amano, Tomohiro Ishii, Hidenori Haruna, Maki Igarashi, Masafumi Kon, Ryuji Fukuzawa, Yukichi Tanaka, Maki Fukami, Tomonobu Hasegawa, Satoshi Narumi
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency. PloS one 13 (11) (2018)
Benjamin J Halliday, Ryuji Fukuzawa, David M Markie, Richard G Grundy, Jackie L Ludgate, Michael A Black, Jane E Skeen, Robert J Weeks, Daniel R Catchpoole, Aedan G K Roberts, Anthony E Reeve, Ian M Morison
Germline mutations and somatic inactivation of TRIM28 in Wilms tumour. PLoS genetics 14 (6) (2018)
Ryuji Fukuzawa, Matthew R Anaka, Ian M Morison, Anthony E Reeve
The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour. PloS one 12 (10) (2017)

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