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Kayoko Saito

Showing results (1-10 of 152) with videos related to

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No to Shinkei = Brain and Nerve|February 26, 2005
[Prenatal diagnosis for neuromuscular diseases]Kayoko Saito
No to Hattatsu = Brain and Development|June 16, 2006
[Consideration of preimplantation genetic diagnosis from a pediatrician's point of view]Kayoko Saito
No to Hattatsu = Brain and Development|November 22, 2007
[Genetic counseling in child neurology]Kayoko Saito
Prenatal Diagnosis|March 30, 2006
Prenatal diagnosis of Fukuyama congenital muscular dystrophyKayoko Saito
Nihon Rinsho. Japanese Journal of Clinical Medicine|October 28, 2010
[Carrier diagnosis and genetic counseling]Kayoko Saito
Brain & Development|August 1, 2002
Bibliography of congenital muscular dystrophies: Series IV (2000) with Appendix IIYukio Fukuyama, Kayoko Saito
Brain & Development|March 21, 2003
Bibliography of congenital muscular dystrophies: Series V (2001)Yukio Fukuyama, Kayoko Saito
Journal of Human Genetics|February 27, 2015
A new method for SMN1 and hybrid SMN gene analysis in spinal muscular atrophy using long-range PCR followed by sequencingYuji Kubo, Hisahide Nishio, Kayoko Saito
American Journal of Medical Genetics. Part A|July 18, 2009
A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delayKeiko Shimojima, Kayoko Saito, Toshiyuki Yamamoto
Seikagaku. the Journal of Japanese Biochemical Society|May 4, 2012
[Cell fusion as a key mechanism for cell-based therapy towards Duchenne muscular dystrophy]Akihiro Umezawa, Yayoi Kawamichi, Kayoko Saito
Pageof 16

Showing results (1-10 of 152) with videos related to

Sort By:
Pageof 16
No to Shinkei = Brain and Nerve|February 26, 2005
[Prenatal diagnosis for neuromuscular diseases]Kayoko Saito
No to Hattatsu = Brain and Development|June 16, 2006
[Consideration of preimplantation genetic diagnosis from a pediatrician's point of view]Kayoko Saito
No to Hattatsu = Brain and Development|November 22, 2007
[Genetic counseling in child neurology]Kayoko Saito
Prenatal Diagnosis|March 30, 2006
Prenatal diagnosis of Fukuyama congenital muscular dystrophyKayoko Saito
Nihon Rinsho. Japanese Journal of Clinical Medicine|October 28, 2010
[Carrier diagnosis and genetic counseling]Kayoko Saito
Brain & Development|August 1, 2002
Bibliography of congenital muscular dystrophies: Series IV (2000) with Appendix IIYukio Fukuyama, Kayoko Saito
Brain & Development|March 21, 2003
Bibliography of congenital muscular dystrophies: Series V (2001)Yukio Fukuyama, Kayoko Saito
Journal of Human Genetics|February 27, 2015
A new method for SMN1 and hybrid SMN gene analysis in spinal muscular atrophy using long-range PCR followed by sequencingYuji Kubo, Hisahide Nishio, Kayoko Saito
American Journal of Medical Genetics. Part A|July 18, 2009
A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delayKeiko Shimojima, Kayoko Saito, Toshiyuki Yamamoto
Seikagaku. the Journal of Japanese Biochemical Society|May 4, 2012
[Cell fusion as a key mechanism for cell-based therapy towards Duchenne muscular dystrophy]Akihiro Umezawa, Yayoi Kawamichi, Kayoko Saito
Pageof 16