Ovarian dysfunction in women with Turner syndrome by Maki Fukami

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Precocious Puberty in Boys with <em>NR0B1</em> Variants by Atsushi Hattori, Maki Fukami

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Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders by Maki Fukami, Mami Miyado

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Mosaic loss of the Y chromosome and men's health by Maki Fukami, Mami Miyado

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Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development by Atsushi Hattori, Maki Fukami

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SHOX and sex difference in height: a hypothesis by Tsutomu Ogata, Atsushi Hattori, Maki Fukami

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Molecular Bases and Phenotypic Determinants of Aromatase Excess Syndrome by Maki Fukami, Makio Shozu, Tsutomu Ogata

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Genetic variants of G‐protein coupled receptors associated with pubertal disorders by Erina Suzuki, Mami Miyado, Yoko Kuroki, Maki Fukami

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Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disorders by Yoko Kuroki, Atsushi Hattori, Keiko Matsubara, Maki Fukami

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Case of heterotopic cervical pregnancy and total placenta accreta after artificial cycle frozen‐thawed embryo transfer by Kazuki Saito, Maki Fukami, Mami Miyado, Ichiro Ono, Keijiro Sumori

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Efficient Superovulation and Egg Collection from Mice by Miyuki Shindo, Kenji Miyado, Woojin Kang, Maki Fukami, Mami Miyado

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Mamld1 knockdown reduces testosterone production and Cyp17a1 expression in mouse Leydig tumor cells. by Michiko Nakamura, Maki Fukami, Fumihiro Sugawa, Mami Miyado, Katsuya Nonomura, Tsutomu Ogata

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Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short stature by Hibiki Doi, Ikuko Kageyama, Yuko Katoh-Fukui, Atsushi Hattori, Maki Fukami, Naoto Shimura

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Coffin‐Lowry syndrome in a girl with 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 disruption by whole genome sequencing by Kaori Yamoto, Hirotomo Saitsu, Yasuko Fujisawa, Fumiko Kato, Keiko Matsubara, Maki Fukami, Masayo Kagami, Tsutomu Ogata

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GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly by Maki Igarashi, Kentaro Mizuno, Masafumi Kon, Satoshi Narumi, Yoshiyuki Kojima, Yutaro Hayashi, Tsutomu Ogata, Maki Fukami

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DNA methylation changes in the genome of patients with hypogonadotropic hypogonadism by Erina Suzuki, Kazuhiko Nakabayashi, Saki Aoto, Tsutomu Ogata, Yoko Kuroki, Mami Miyado, Maki Fukami, Keiko Matsubara

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Copy‐number analysis of Y‐linked loci in young men with non‐obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome Y by Erina Suzuki, Yoshitomo Kobori, Momori Katsumi, Kikumi Ushijima, Toru Uchiyama, Hiroshi Okada, Mami Miyado, Maki Fukami

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Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome by Atsushi Hattori, Torayuki Okuyama, Tetsumin So, Motomichi Kosuga, Keiko Ichimoto, Kei Murayama, Masayo Kagami, Maki Fukami, Yasuyuki Fukuhara

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Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR by Masayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, Kentaro Matsuoka, Akie Nakamura, Keiko Matsubara, Kazuhiko Nakabayashi, Shuji Takada, Maki Fukami, Tsutomu Ogata

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Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene by Hiroyuki Ono, Hirotomo Saitsu, Reiko Horikawa, Shinichi Nakashima, Yumiko Ohkubo, Kumiko Yanagi, Kazuhiko Nakabayashi, Maki Fukami, Yasuko Fujisawa, Tsutomu Ogata

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