Publications by authors named "Masae Ono"

Claim this Profile
E
Establishing intellectual disability as the key feature of patients with biallelic RNPC3 variants.
Mamiko Yamada, Masae Ono, Tomohiro Ishii, Hisato Suzuki, Tomoko Uehara

Am J Med Genet A· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Low risk of treatment resistance in Down syndrome with Kawasaki disease.
Shinichi Takatsuki, Shohei Ogata, Masahiro Ishii, Masato Yokozawa, Masae Ono, Junko Shiono

Pediatr Int· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Incidence of febrile seizure in patients with Down syndrome.
Shuichi Shimakawa, Takuya Tanabe, Masae Ono, Michiko Nonaka, Mitsuhiko Nambu

Pediatr Int· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo mutations in the BMPR2 gene in patients with heritable pulmonary arterial hypertension.
Yuichi Momose, Yuki Aimi, Tomomi Hirayama, Masaharu Kataoka, Masae Ono

Ann Hum Genet· March 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Presymptomatic genetic analysis during pregnancy for vascular type Ehlers-Danlos syndrome.
Banyar Than Naing, Atsushi Watanabe, Shinji Tanigaki, Masae Ono, Mitsutoshi Iwashita

Int Med Case Rep J· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Alu-mediated nonallelic homologous and nonhomologous recombination in the BMPR2 gene in heritable pulmonary arterial hypertension.
Masaharu Kataoka, Yuki Aimi, Ryoji Yanagisawa, Masae Ono, Akira Oka

Genet Med· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.
Shin Hayashi, Issei Imoto, Yoshinori Aizu, Nobuhiko Okamoto, Seiji Mizuno, Masae Ono, Hiroaki Ono

J Hum Genet· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array-based comparative genomic hybridization.
Shin Hayashi, Masae Ono, Yoshio Makita, Issei Imoto, Shuki Mizutani

Am J Med Genet A· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Epidemic hepatitis A in Japan: background and actions to be taken].
Naoaki Hashimoto, Masae Ono

Nihon Rinsho· August 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis