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Gen Nishimura

Showing results (71-80 of 334) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal featuresTsutomu Ogata, Koji Muroya, Goro Sasaki, et al.
Brain & Development|March 2, 2005
Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type IIHiroshi Ozawa, Chikako Takayama, Akira Nishida, et al.
Pediatric Radiology|April 26, 2012
Prenatal diagnosis of fetal skeletal dysplasia with 3D CTOsamu Miyazaki, Gen Nishimura, Haruhiko Sago, et al.
Journal of Human Genetics|March 14, 2007
The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressivaMasahiro Nakajima, Nobuhiko Haga, Kazuharu Takikawa, et al.
Japanese Journal of Clinical Oncology|August 1, 2008
Patterns of local recurrence after intraoperative radiotherapy for advanced neuroblastomaEtsuo Kunieda, Seiichi Hirobe, Takashi Kaneko, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Femoral-tibial-digital malformations in a boy with the Japanese founder triplication of BHLHA9Eiko Nagata, Nobuhiko Haga, Yasuko Fujisawa, et al.
American Journal of Medical Genetics. Part A|April 18, 2025
A Case of Penttinen Syndrome With Radiographic Acroosteolysis From Age 3 YearsKazuhiro Shimura, Machiko Toki, Yuko Tsujioka, et al.
American Journal of Medical Genetics|October 26, 2002
Autopsy case of microcephalic osteodysplastic primordial "dwarfism" type IIRyuji Fukuzawa, Seiji Sato, Michael J Sullivan, et al.
Skeletal Radiology|June 10, 2006
Achondroplasia and enchondromatosis: report of three boysChikahiko Numakura, Hironori Kobayashi, Yukihiro Hasegawa, et al.
Japanese Journal of Radiology|October 25, 2021
A primer on skeletal dysplasiasAtsuhiko Handa, Gen Nishimura, Malia Xin Zhan, et al.
Pageof 34

Showing results (71-80 of 334) with videos related to

Sort By:
Pageof 34
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal featuresTsutomu Ogata, Koji Muroya, Goro Sasaki, et al.
Brain & Development|March 2, 2005
Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type IIHiroshi Ozawa, Chikako Takayama, Akira Nishida, et al.
Pediatric Radiology|April 26, 2012
Prenatal diagnosis of fetal skeletal dysplasia with 3D CTOsamu Miyazaki, Gen Nishimura, Haruhiko Sago, et al.
Journal of Human Genetics|March 14, 2007
The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressivaMasahiro Nakajima, Nobuhiko Haga, Kazuharu Takikawa, et al.
Japanese Journal of Clinical Oncology|August 1, 2008
Patterns of local recurrence after intraoperative radiotherapy for advanced neuroblastomaEtsuo Kunieda, Seiichi Hirobe, Takashi Kaneko, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Femoral-tibial-digital malformations in a boy with the Japanese founder triplication of BHLHA9Eiko Nagata, Nobuhiko Haga, Yasuko Fujisawa, et al.
American Journal of Medical Genetics. Part A|April 18, 2025
A Case of Penttinen Syndrome With Radiographic Acroosteolysis From Age 3 YearsKazuhiro Shimura, Machiko Toki, Yuko Tsujioka, et al.
American Journal of Medical Genetics|October 26, 2002
Autopsy case of microcephalic osteodysplastic primordial "dwarfism" type IIRyuji Fukuzawa, Seiji Sato, Michael J Sullivan, et al.
Skeletal Radiology|June 10, 2006
Achondroplasia and enchondromatosis: report of three boysChikahiko Numakura, Hironori Kobayashi, Yukihiro Hasegawa, et al.
Japanese Journal of Radiology|October 25, 2021
A primer on skeletal dysplasiasAtsuhiko Handa, Gen Nishimura, Malia Xin Zhan, et al.
Pageof 34