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Gen Nishimura

Showing results (41-50 of 334) with videos related to

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American Journal of Medical Genetics|January 25, 2002
Intrafamilial phenotypic variations in cranioectodermal dysplasia: propositus with typical manifestations and her brother with perinatal deathShinya Tamai, Masahiro Tojo, Tsutomu Kamimaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 1, 2021
Development of individuals with thanatophoric dysplasia surviving beyond infancyMariko Ushioda, Hideaki Sawai, Hironao Numabe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 24, 2018
Myhre syndrome: Age-dependent progressive phenotypeRisa Nomura, Kentaro Miyai, Gen Nishimura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 28, 2018
Cyclic intravenous pamidronate in a very low-birthweight infant with osteogenesis imperfectaShohei Eto, Satoshi Hada, Rie Fukuhara, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 11, 2016
A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1Shinji Higuchi, Masaki Takagi, Satoshi Shimomura, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Atypical achondroplasia due to somatic mosaicism for the common thanatophoric dysplasia mutation R248CMasaki Takagi, Saori Kaneko-Schmitt, Nobuhiro Suzumori, et al.
AJR. American Journal of Roentgenology|September 23, 2003
Contrast-enhanced MRI of an early preosseous lesion of fibrodysplasia ossificans progressiva in a 21-month-old boyHiroaki Hagiwara, Noriko Aida, Jiro Machida, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 18, 2010
Hajdu-Cheney syndrome: infantile onset of hydrocephalus and serpentine fibulaeRieko Takatani, Tomohiro Someya, Itsuro Kazukawa, et al.
American Journal of Medical Genetics. Part A|August 5, 2015
Progressive hip joint subluxation in Saul-Wilson syndromeYasutsugu Chinen, Takuya Kaneshi, Takeshi Kamiya, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Czech dysplasia occurring in a Japanese familyYoshito Matsui, Toshimi Michigami, Kanako Tachikawa, et al.
Pageof 34

Showing results (41-50 of 334) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics|January 25, 2002
Intrafamilial phenotypic variations in cranioectodermal dysplasia: propositus with typical manifestations and her brother with perinatal deathShinya Tamai, Masahiro Tojo, Tsutomu Kamimaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 1, 2021
Development of individuals with thanatophoric dysplasia surviving beyond infancyMariko Ushioda, Hideaki Sawai, Hironao Numabe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 24, 2018
Myhre syndrome: Age-dependent progressive phenotypeRisa Nomura, Kentaro Miyai, Gen Nishimura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 28, 2018
Cyclic intravenous pamidronate in a very low-birthweight infant with osteogenesis imperfectaShohei Eto, Satoshi Hada, Rie Fukuhara, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 11, 2016
A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1Shinji Higuchi, Masaki Takagi, Satoshi Shimomura, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Atypical achondroplasia due to somatic mosaicism for the common thanatophoric dysplasia mutation R248CMasaki Takagi, Saori Kaneko-Schmitt, Nobuhiro Suzumori, et al.
AJR. American Journal of Roentgenology|September 23, 2003
Contrast-enhanced MRI of an early preosseous lesion of fibrodysplasia ossificans progressiva in a 21-month-old boyHiroaki Hagiwara, Noriko Aida, Jiro Machida, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 18, 2010
Hajdu-Cheney syndrome: infantile onset of hydrocephalus and serpentine fibulaeRieko Takatani, Tomohiro Someya, Itsuro Kazukawa, et al.
American Journal of Medical Genetics. Part A|August 5, 2015
Progressive hip joint subluxation in Saul-Wilson syndromeYasutsugu Chinen, Takuya Kaneshi, Takeshi Kamiya, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Czech dysplasia occurring in a Japanese familyYoshito Matsui, Toshimi Michigami, Kanako Tachikawa, et al.
Pageof 34