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Plos One|July 18, 2013
Cryptic genomic rearrangements in three patients with 46,XY disorders of sex developmentMaki Igarashi, Vu Chi Dung, Erina Suzuki, et al.Sexual Medicine|November 15, 2023
Variations in gender identity and sexual orientation of university studentsTomoko Yoshida, Keiko Matsubara, Hiroko Ogata-Kawata, et al.The Journal of Steroid Biochemistry and Molecular Biology|February 16, 2016
Steroidogenic pathways involved in androgen biosynthesis in eumenorrheic women and patients with polycystic ovary syndromeKazuki Saito, Toshiya Matsuzaki, Takeshi Iwasa, et al.Journal of Pediatric Gastroenterology and Nutrition|January 27, 2022
Quantification of Maternal Microchimeric Cells in the Liver of Children With Biliary AtresiaSatoshi Tamaoka, Akinari Fukuda, Yuko Katoh-Fukui, et al.The Journal of Clinical Endocrinology and Metabolism|August 12, 2025
Association Between Particulate Matter Exposure and Thyroid Hormone Levels in Early Childhood: Results from JECSLimin Yang, Miori Sato, Mayako Saito-Abe, et al.Environmental Research|September 7, 2025
Maternal blood metal levels during pregnancy and body mass index z-score, overweight, and obesity among children: Findings of the Japan Environment and Children's StudyLimin Yang, Miori Sato, Mayako Saito-Abe, et al.Journal of Human Genetics|June 5, 2015
Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short statureMaki Fukami, Yasuhiro Naiki, Koji Muroya, et al.EMBO Molecular Medicine|November 19, 2016
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiencyAntonino Montalbano, Lonny Juergensen, Ralph Roeth, et al.Journal of Human Genetics|February 28, 2021
Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndromeSachiko Nishina, Katsuhiro Hosono, Shizuka Ishitani, et al.Clinical Epigenetics|February 3, 2026
Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding siteHayate Masubuchi, Tatsuki Urakawa, Rika Kosaki, et al.Pageof 32