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Molecular Biology Reports
|
March 5, 2014
Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome
Hui Ram Kim, Mee Hyun Song, Min-A Kim, et al.
Biochemical and Biophysical Research Communications
|
December 15, 2010
Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms
Mee Hyun Song, Soo-Young Choi, Ling Wu, et al.
Cells
|
September 28, 2023
Novel Variant in <i>CEP250</i> Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss
Minjin Kang, Jung Ah Kim, Mee Hyun Song, et al.
Clinical Anatomy (New York, N.Y.)
|
November 1, 2005
Surgical anatomy of the middle turbinate
Hye Yeon Lee, Chang-Hoon Kim, Jin Young Kim, et al.
Gene
|
April 9, 2013
Genetic analysis of auditory neuropathy spectrum disorder in the Korean population
Seung-Hyun Bae, Jeong-In Baek, Jong Dae Lee, et al.
Physiological Genomics
|
August 13, 2009
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein
Hee Keun Lee, Mee Hyun Song, Myengmo Kang, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Molecular Biology Reports
|
March 5, 2014
Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome
Hui Ram Kim, Mee Hyun Song, Min-A Kim, et al.
Biochemical and Biophysical Research Communications
|
December 15, 2010
Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms
Mee Hyun Song, Soo-Young Choi, Ling Wu, et al.
Cells
|
September 28, 2023
Novel Variant in <i>CEP250</i> Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss
Minjin Kang, Jung Ah Kim, Mee Hyun Song, et al.
Clinical Anatomy (New York, N.Y.)
|
November 1, 2005
Surgical anatomy of the middle turbinate
Hye Yeon Lee, Chang-Hoon Kim, Jin Young Kim, et al.
Gene
|
April 9, 2013
Genetic analysis of auditory neuropathy spectrum disorder in the Korean population
Seung-Hyun Bae, Jeong-In Baek, Jong Dae Lee, et al.
Physiological Genomics
|
August 13, 2009
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein
Hee Keun Lee, Mee Hyun Song, Myengmo Kang, et al.
Page
of 5