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Satomi Koyama
Satomi Koyama
Tokyo Medical and Dental University
Endocrinology
Internal medicine
Compound heterozygosity
Congenital adrenal hyperplasia
Structural gene
3
Papers
36
Citations
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2024
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Genetic Analysis of Japanese Patients with 21-Hydroxylase Deficiency: Identification of a Patient with a New Mutation of a Homozygous Deletion of Adenine at Codon 246 and Patients without Demonstrable Mutations within the Structural Gene for CYP21
2002
The Journal of Clinical Endocrinology and Metabolism
Satomi Koyama
Takio Toyoura
Sumitaka Saisho
Kazuhiko Shimozawa
Junichi Yata
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Citations (34)
A highly specific heterologous enzyme immunoassay for 5α-androstane-3α, 17β-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretions
2002
Steroids
Toshikazu Onishi
Hajime Takei
Akira Kambegawa
Sumitaka Saisho
Kenichi Kashimada
Satomi Koyama
Shuki Mizutani
Pemmaraju N. Rao
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Citations (2)
91 Case report : Metaphyseal Dysplasia Simulating Cartilage Hair Hypoplasia
2002
Clinical Pediatric Endocrinology
Kenichi Kashimada
Makoto Ono
T. Ohnishi
Satomi Koyama
Takio Toyoura
Sumitaka Saisho
Kazuhiko Shimozawa
Shuki Mizutani
S Ikegawa
Gen Nishimura
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