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The Journal of Craniofacial Surgery
|
October 5, 2021
Airway Compromise in Mandibular Fracture
Ryo Sasaki, Chika Togashi, Noriko Sangu Miyamoto, et al.
Epilepsy Research
|
November 13, 2015
Characteristics of patients with benign partial epilepsy in infancy without PRRT2 mutations
Noriko Sangu, Keiko Shimojima, Okumura Akihisa, et al.
The Journal of Craniofacial Surgery
|
October 20, 2018
Genial Tubercle Fracture
Ryo Sasaki, Toshihiro Okamoto, Noriko Sangu, et al.
Congenital Anomalies
|
April 23, 2014
Growth patterns of patients with 1p36 deletion syndrome
Noriko Sangu, Keiko Shimojima, Shino Shimada, et al.
Plastic and Reconstructive Surgery. Global Open
|
June 23, 2023
Innsbruck-style Retromandibular Anterior Trans-parotid Approach for Condylar Fractures: A Retrospective Review of 39 Fractures
Ryo Sasaki, Yorikatsu Watanabe, Noriko Sangu Miyamoto, et al.
American Journal of Medical Genetics. Part A
|
March 5, 2015
An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation
Keiko Shimojima, Nobuhiko Okamoto, Akiko Tamasaki, et al.
American Journal of Medical Genetics. Part A
|
December 21, 2013
Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4
Toshiyuki Yamamoto, Masami Togawa, Shino Shimada, et al.
Human Genome Variation
|
February 23, 2017
A 7q31.33q32.1 microdeletion including <i>LRRC4</i> and <i>GRM8</i> is associated with severe intellectual disability and characteristics of autism
Noriko Sangu, Keiko Shimojima, Yuya Takahashi, et al.
European Journal of Medical Genetics
|
July 21, 2015
Leukoencephalopathy associated with 11q24 deletion involving the gene encoding hepatic and glial cell adhesion molecule in two patients
Toshiyuki Yamamoto, Shino Shimada, Keiko Shimojima, et al.
Human Genome Variation
|
June 9, 2016
A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene
Noriko Sangu, Nobuhiko Okamoto, Keiko Shimojima, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
The Journal of Craniofacial Surgery
|
October 5, 2021
Airway Compromise in Mandibular Fracture
Ryo Sasaki, Chika Togashi, Noriko Sangu Miyamoto, et al.
Epilepsy Research
|
November 13, 2015
Characteristics of patients with benign partial epilepsy in infancy without PRRT2 mutations
Noriko Sangu, Keiko Shimojima, Okumura Akihisa, et al.
The Journal of Craniofacial Surgery
|
October 20, 2018
Genial Tubercle Fracture
Ryo Sasaki, Toshihiro Okamoto, Noriko Sangu, et al.
Congenital Anomalies
|
April 23, 2014
Growth patterns of patients with 1p36 deletion syndrome
Noriko Sangu, Keiko Shimojima, Shino Shimada, et al.
Plastic and Reconstructive Surgery. Global Open
|
June 23, 2023
Innsbruck-style Retromandibular Anterior Trans-parotid Approach for Condylar Fractures: A Retrospective Review of 39 Fractures
Ryo Sasaki, Yorikatsu Watanabe, Noriko Sangu Miyamoto, et al.
American Journal of Medical Genetics. Part A
|
March 5, 2015
An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation
Keiko Shimojima, Nobuhiko Okamoto, Akiko Tamasaki, et al.
American Journal of Medical Genetics. Part A
|
December 21, 2013
Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4
Toshiyuki Yamamoto, Masami Togawa, Shino Shimada, et al.
Human Genome Variation
|
February 23, 2017
A 7q31.33q32.1 microdeletion including <i>LRRC4</i> and <i>GRM8</i> is associated with severe intellectual disability and characteristics of autism
Noriko Sangu, Keiko Shimojima, Yuya Takahashi, et al.
European Journal of Medical Genetics
|
July 21, 2015
Leukoencephalopathy associated with 11q24 deletion involving the gene encoding hepatic and glial cell adhesion molecule in two patients
Toshiyuki Yamamoto, Shino Shimada, Keiko Shimojima, et al.
Human Genome Variation
|
June 9, 2016
A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene
Noriko Sangu, Nobuhiko Okamoto, Keiko Shimojima, et al.
Page
of 3