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Gen Nishimura

Showing results (21-30 of 334) with videos related to

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American Journal of Medical Genetics. Part A|July 26, 2017
Additional report on Moreno-Nishimura-Schmidt overgrowth syndromeAtsuhiko Handa, Koji Muroya, Tomohiro Ishii, et al.
Journal of Pediatric Genetics|August 11, 2017
Severe Form of Brachydactyly Type A1 in a Child with a c.298G > A Mutation in <i>IHH</i> GeneSmrithi Salian, Anju Shukla, Gen Nishimura, et al.
Clinical Dysmorphology|July 19, 2003
Ischiospinal dysostosis with cystic kidney disease: report of two casesGen Nishimura, Ok Hwa Kim, Seiji Sato, et al.
Pediatric Radiology|April 17, 2002
Prenatal diagnosis of hypochondrogenesis using fetal MRI: a case reportHiroshi Suzumura, Tatsuo Kohno, Gen Nishimura, et al.
American Journal of Medical Genetics. Part A|November 10, 2011
Submicroscopic deletion of 12q13 including HOXC gene cluster with skeletal anomalies and global developmental delayNobuhiko Okamoto, Daisuke Tamura, Gen Nishimura, et al.
Japanese Journal of Radiology|January 23, 2020
Skeletal ciliopathies: a pattern recognition approachAtsuhiko Handa, Ulrika Voss, Anna Hammarsjö, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 23, 2020
A novel <i>NPR2</i> mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type MaroteauxNaoko Amano, Hiroshi Kitoh, Satoshi Narumi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 27, 2015
Painless lumps in the proximal interphalangeal joints in tricho-rhino-phalangeal syndrome type 1Takako Miyamae, Gen Nishimura, Takayuki Kishi, et al.
Pediatric Radiology|September 7, 2007
Prenatal diagnosis of chondrodysplasia punctata tibia-metacarpal type using multidetector CT and three-dimensional reconstructionOsamu Miyazaki, Gen Nishimura, Haruhiko Sago, et al.
Fetal Diagnosis and Therapy|November 7, 2008
Prenatal diagnosis of thanatophoric dysplasia by 3-D helical computed tomography and genetic analysisSeiji Tsutsumi, Hideaki Sawai, Gen Nishimura, et al.
Pageof 34

Showing results (21-30 of 334) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics. Part A|July 26, 2017
Additional report on Moreno-Nishimura-Schmidt overgrowth syndromeAtsuhiko Handa, Koji Muroya, Tomohiro Ishii, et al.
Journal of Pediatric Genetics|August 11, 2017
Severe Form of Brachydactyly Type A1 in a Child with a c.298G > A Mutation in <i>IHH</i> GeneSmrithi Salian, Anju Shukla, Gen Nishimura, et al.
Clinical Dysmorphology|July 19, 2003
Ischiospinal dysostosis with cystic kidney disease: report of two casesGen Nishimura, Ok Hwa Kim, Seiji Sato, et al.
Pediatric Radiology|April 17, 2002
Prenatal diagnosis of hypochondrogenesis using fetal MRI: a case reportHiroshi Suzumura, Tatsuo Kohno, Gen Nishimura, et al.
American Journal of Medical Genetics. Part A|November 10, 2011
Submicroscopic deletion of 12q13 including HOXC gene cluster with skeletal anomalies and global developmental delayNobuhiko Okamoto, Daisuke Tamura, Gen Nishimura, et al.
Japanese Journal of Radiology|January 23, 2020
Skeletal ciliopathies: a pattern recognition approachAtsuhiko Handa, Ulrika Voss, Anna Hammarsjö, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 23, 2020
A novel <i>NPR2</i> mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type MaroteauxNaoko Amano, Hiroshi Kitoh, Satoshi Narumi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 27, 2015
Painless lumps in the proximal interphalangeal joints in tricho-rhino-phalangeal syndrome type 1Takako Miyamae, Gen Nishimura, Takayuki Kishi, et al.
Pediatric Radiology|September 7, 2007
Prenatal diagnosis of chondrodysplasia punctata tibia-metacarpal type using multidetector CT and three-dimensional reconstructionOsamu Miyazaki, Gen Nishimura, Haruhiko Sago, et al.
Fetal Diagnosis and Therapy|November 7, 2008
Prenatal diagnosis of thanatophoric dysplasia by 3-D helical computed tomography and genetic analysisSeiji Tsutsumi, Hideaki Sawai, Gen Nishimura, et al.
Pageof 34