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Seiji Mizuno

Showing results (1-10 of 111) with videos related to

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Nanoscale Research Letters|August 25, 2012
Acoustic phonon modes and phononic bandgaps in GaN/AlN nanowire superlatticesSeiji Mizuno
Journal of Physics. Condensed Matter : an Institute of Physics Journal|August 10, 2011
Acoustic phonon modes and dispersion relations of nanowire superlatticesSeiji Mizuno, Norihiko Nishiguchi
No to Hattatsu = Brain and Development|September 18, 2010
[Intervention to reduce the difficulty in kanji copying related to the visuo-spatial dysfunction in patients with Williams syndrome]Miho Nakamura, Seiji Mizuno, Toshiyuki Kumagai
American Journal of Medical Genetics. Part A|February 1, 2018
Growth pattern of Rahman syndromeToshiki Takenouchi, Tomoko Uehara, Kenjiro Kosaki, et al.
Brain & Development|October 4, 2016
Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23Yukako Muramatsu, Yoshihito Tokita, Seiji Mizuno, et al.
Congenital Anomalies|May 21, 2005
Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutationSeiji Mizuno, Yasukazu Yamada, Kenichiro Yamada, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock-Carey syndrome phenotypeToshiki Takenouchi, Kiyokuni Miura, Tomoko Uehara, et al.
Journal of Human Genetics|November 1, 2020
A novel missense variant in CUL3 shows altered binding ability to BTB-adaptor proteins leading to diverse phenotypes of CUL3-related disordersKohji Kato, Fuyuki Miya, Yasuyoshi Oka, et al.
Frontiers in Human Neuroscience|December 31, 2013
Developmental changes in mental rotation ability and visual perspective-taking in children and adults with Williams syndromeMasahiro Hirai, Yukako Muramatsu, Seiji Mizuno, et al.
European Journal of Medical Genetics|December 10, 2017
Redefining the phenotypic spectrum of de novo heterozygous CDK13 variants: Three patients without cardiac defectsTomoko Uehara, Toshiki Takenouchi, Rika Kosaki, et al.
Pageof 12

Showing results (1-10 of 111) with videos related to

Sort By:
Pageof 12
Nanoscale Research Letters|August 25, 2012
Acoustic phonon modes and phononic bandgaps in GaN/AlN nanowire superlatticesSeiji Mizuno
Journal of Physics. Condensed Matter : an Institute of Physics Journal|August 10, 2011
Acoustic phonon modes and dispersion relations of nanowire superlatticesSeiji Mizuno, Norihiko Nishiguchi
No to Hattatsu = Brain and Development|September 18, 2010
[Intervention to reduce the difficulty in kanji copying related to the visuo-spatial dysfunction in patients with Williams syndrome]Miho Nakamura, Seiji Mizuno, Toshiyuki Kumagai
American Journal of Medical Genetics. Part A|February 1, 2018
Growth pattern of Rahman syndromeToshiki Takenouchi, Tomoko Uehara, Kenjiro Kosaki, et al.
Brain & Development|October 4, 2016
Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23Yukako Muramatsu, Yoshihito Tokita, Seiji Mizuno, et al.
Congenital Anomalies|May 21, 2005
Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutationSeiji Mizuno, Yasukazu Yamada, Kenichiro Yamada, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock-Carey syndrome phenotypeToshiki Takenouchi, Kiyokuni Miura, Tomoko Uehara, et al.
Journal of Human Genetics|November 1, 2020
A novel missense variant in CUL3 shows altered binding ability to BTB-adaptor proteins leading to diverse phenotypes of CUL3-related disordersKohji Kato, Fuyuki Miya, Yasuyoshi Oka, et al.
Frontiers in Human Neuroscience|December 31, 2013
Developmental changes in mental rotation ability and visual perspective-taking in children and adults with Williams syndromeMasahiro Hirai, Yukako Muramatsu, Seiji Mizuno, et al.
European Journal of Medical Genetics|December 10, 2017
Redefining the phenotypic spectrum of de novo heterozygous CDK13 variants: Three patients without cardiac defectsTomoko Uehara, Toshiki Takenouchi, Rika Kosaki, et al.
Pageof 12