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Cytogenetic and Genome Research|May 13, 2020
Established and Novel Mechanisms Leading to de novo Genomic Rearrangements in the Human GermlineAtsushi Hattori, Maki FukamiMethods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Multifocal Genomic Reconstruction Leading to Germline Structural VariantsAtsushi Hattori, Maki FukamiBiomolecules|May 16, 2023
Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular DevelopmentAtsushi Hattori, Maki FukamiEndocrine Journal|July 10, 2024
SHOX and sex difference in height: a hypothesisTsutomu Ogata, Atsushi Hattori, Maki FukamiAnnals of Pediatric Endocrinology & Metabolism|July 3, 2024
Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disordersYoko Kuroki, Atsushi Hattori, Keiko Matsubara, et al.Endocrine Journal|December 22, 2024
Intragenic duplication of PHEX in a girl with X-linked hypophosphatemia: a case report with review of literatureKazuhisa Akiba, Keiko Matsubara, Atsushi Hattori, et al.Cytogenetic and Genome Research|July 2, 2025
Clustered Structural Variants Involving PHEX at Xp22 in a Female Patient with X-Linked HypophosphatemiaErika Uehara, Yasuhiro Naiki, Atsushi Hattori, et al.Human Genome Variation|July 26, 2024
Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short statureHibiki Doi, Ikuko Kageyama, Yuko Katoh-Fukui, et al.Human Genome Variation|February 3, 2021
NDNF variants are rare in patients with congenital hypogonadotropic hypogonadismSatoshi Tamaoka, Erina Suzuki, Atsushi Hattori, et al.Sexual Medicine|August 19, 2025
Association between repeat number polymorphisms of sex hormone-related genes and gender phenotype variations in university studentsMizuho Igarashi, Yuko Katoh-Fukui, Atsushi Hattori, et al.Pageof 35