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Gen Nishimura

Showing results (91-100 of 334) with videos related to

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Pediatrics International : Official Journal of the Japan Pediatric Society|June 28, 2019
National survey of prevalence and prognosis of thanatophoric dysplasia in JapanHideaki Sawai, Kaname Oka, Mariko Ushioda, et al.
Clinical Rheumatology|January 28, 2006
Intrafamilial phenotypic diversity in multiple epiphyseal dysplasia associated with a COL9A2 mutation (EDM2)Mitsuhiko Takahashi, Yoshito Matsui, Tomohiro Goto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 13, 2010
Bifid epiglottis: syndromic constituent rather than isolated anomalyHaruko Tsurumi, Masaki Ito, Kenji Ishikura, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
Nevo syndrome with an NSD1 deletion: a variant of Sotos syndrome?Nobuko Kanemoto, Katsuyoshi Kanemoto, Gen Nishimura, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Radiological evolution in IMAGe association: a case reportNaoko Amano, Hori Naoaki, Tomohiro Ishii, et al.
Congenital Anomalies|March 16, 2018
Familial campomelic dysplasia due to maternal germinal mosaicismDaisuke Higeta, Rie Yamaguchi, Takeshi Takagi, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Metaphyseal dysplasia of Braun-Tinschert type: report of a Japanese girlShinjiro Takata, Gen Nishimura, Shiro Ikegawa, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 9, 2008
Nephrotic state as a risk factor for developing posterior reversible encephalopathy syndrome in paediatric patients with nephrotic syndromeKenji Ishikura, Masahiro Ikeda, Yuko Hamasaki, et al.
Human Genetics|January 30, 2004
Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndromeEiji Nakashima, Akihiko Mabuchi, Yoshio Makita, et al.
Human Genetics|March 31, 2007
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese familyYoshinari Miyamoto, Tatsuo Matsuda, Hiroshi Kitoh, et al.
Pageof 34

Showing results (91-100 of 334) with videos related to

Sort By:
Pageof 34
Pediatrics International : Official Journal of the Japan Pediatric Society|June 28, 2019
National survey of prevalence and prognosis of thanatophoric dysplasia in JapanHideaki Sawai, Kaname Oka, Mariko Ushioda, et al.
Clinical Rheumatology|January 28, 2006
Intrafamilial phenotypic diversity in multiple epiphyseal dysplasia associated with a COL9A2 mutation (EDM2)Mitsuhiko Takahashi, Yoshito Matsui, Tomohiro Goto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 13, 2010
Bifid epiglottis: syndromic constituent rather than isolated anomalyHaruko Tsurumi, Masaki Ito, Kenji Ishikura, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
Nevo syndrome with an NSD1 deletion: a variant of Sotos syndrome?Nobuko Kanemoto, Katsuyoshi Kanemoto, Gen Nishimura, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Radiological evolution in IMAGe association: a case reportNaoko Amano, Hori Naoaki, Tomohiro Ishii, et al.
Congenital Anomalies|March 16, 2018
Familial campomelic dysplasia due to maternal germinal mosaicismDaisuke Higeta, Rie Yamaguchi, Takeshi Takagi, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Metaphyseal dysplasia of Braun-Tinschert type: report of a Japanese girlShinjiro Takata, Gen Nishimura, Shiro Ikegawa, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 9, 2008
Nephrotic state as a risk factor for developing posterior reversible encephalopathy syndrome in paediatric patients with nephrotic syndromeKenji Ishikura, Masahiro Ikeda, Yuko Hamasaki, et al.
Human Genetics|January 30, 2004
Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndromeEiji Nakashima, Akihiko Mabuchi, Yoshio Makita, et al.
Human Genetics|March 31, 2007
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese familyYoshinari Miyamoto, Tatsuo Matsuda, Hiroshi Kitoh, et al.
Pageof 34