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Tomoko Jinno

Showing results (1-10 of 8) with videos related to

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Genome Biology and Evolution|August 14, 2020
Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal RegionMaki Fukami, Yasuko Fujisawa, Hiroyuki Ono, et al.
American Journal of Medical Genetics. Part A|June 23, 2019
SHOX far-downstream copy-number variations involving cis-regulatory nucleotide variants in two sisters with Leri-Weill dyschondrosteosisKenichiro Ogushi, Koji Muroya, Hirohito Shima, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 12, 2014
Skeletal Deformity Associated with SHOX DeficiencyAtsuhito Seki, Tomoko Jinno, Erina Suzuki, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of langer mesomelic dysplasiaTakayoshi Tsuchiya, Minoru Shibata, Hironao Numabe, et al.
Journal of the Endocrine Society|June 7, 2021
<i>SOX10</i> Mutation Screening for 117 Patients with Kallmann SyndromeHirohito Shima, Etsuro Tokuhiro, Shingo Okamoto, 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.
Scientific Reports|March 9, 2022
Collection of 2429 constrained headshots of 277 volunteers for deep learningSaki Aoto, Mayumi Hangai, Hitomi Ueno-Yokohata, et al.
Journal of Human Genetics|March 18, 2016
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosisHirohito Shima, Toshiaki Tanaka, Tsutomu Kamimaki, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genome Biology and Evolution|August 14, 2020
Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal RegionMaki Fukami, Yasuko Fujisawa, Hiroyuki Ono, et al.
American Journal of Medical Genetics. Part A|June 23, 2019
SHOX far-downstream copy-number variations involving cis-regulatory nucleotide variants in two sisters with Leri-Weill dyschondrosteosisKenichiro Ogushi, Koji Muroya, Hirohito Shima, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 12, 2014
Skeletal Deformity Associated with SHOX DeficiencyAtsuhito Seki, Tomoko Jinno, Erina Suzuki, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of langer mesomelic dysplasiaTakayoshi Tsuchiya, Minoru Shibata, Hironao Numabe, et al.
Journal of the Endocrine Society|June 7, 2021
<i>SOX10</i> Mutation Screening for 117 Patients with Kallmann SyndromeHirohito Shima, Etsuro Tokuhiro, Shingo Okamoto, 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.
Scientific Reports|March 9, 2022
Collection of 2429 constrained headshots of 277 volunteers for deep learningSaki Aoto, Mayumi Hangai, Hitomi Ueno-Yokohata, et al.
Journal of Human Genetics|March 18, 2016
Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosisHirohito Shima, Toshiaki Tanaka, Tsutomu Kamimaki, et al.
Pageof 1