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Fertility and Sterility|July 28, 2014
Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadismYoko Izumi, Erina Suzuki, Susumu Kanzaki, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 21, 2016
NR0B1 Frameshift Mutation in a Boy with Idiopathic Central Precocious PubertyHirohito Shima, Shuichi Yatsuga, Akie Nakamura, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|February 23, 2017
[Conversion Surgery for Initially Unresectable Locally Advanced Pancreatic Cancer Following Gemcitabine plus Nab-Paclitaxel - A Case Report]Shuji Nakamoto, Ryo Nishiyama, Takayoshi Kaneda, et al.
Human Genome Variation|January 25, 2019
(Epi)genetic defects of <i>MKRN3</i> are rare in Asian patients with central precocious pubertyErina Suzuki, Hirohito Shima, Masayo Kagami, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9Yuko Katoh-Fukui, Maki Igarashi, Keisuke Nagasaki, et al.
Cytogenetic and Genome Research|June 4, 2019
DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number VariationsKenichiro Ogushi, Atsushi Hattori, Erina Suzuki, et al.
Endocrine Journal|August 4, 2017
Next generation sequencing-based mutation screening of 86 patients with idiopathic short statureAtsushi Hattori, Yuko Katoh-Fukui, Akie Nakamura, et al.
Clinical Journal of Gastroenterology|September 6, 2021
TAFRO syndrome complicated by porto-sinusoidal vascular liver disease with portal hypertension: a case reportManabu Hayashi, Jun Wada, Masashi Fujita, et al.
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