E-LIB Suche - Ergebnisse für: Park, Hong-Joon

1

Identification of novel missense mutation related with non-..:

Kim, Ye-Ri ; Kim, Hye-Min ; Lee, Byeonghyeon...
Genes & Genomics. 45 (2023) 2 - p. 225-230 , 2023

Link: https://doi.org/10.1007/..

2

Identification of a novel splicing mutation within SLC17A8 ..:

Ryu, Nari ; Lee, Seokwon ; Park, Hong-Joon...
Gene. 627 (2017) - p. 233-238 , 2017

Link: https://doi.org/10.1016/..

3

Surgical and Audiologic Comparison Between Sophono and Bone..:

Shin, Joong-Wook ; Kim, Sung Huhn ; Choi, Jae Young...
Clinical and Experimental Otorhinolaryngology. 9 (2016) 1 - p. 21-26 , 2016

Link: https://doi.org/10.21053..

4

Genetic analysis of COL11A2 in Korean patients with autosom..:

Kim, Sang-Joo ; Park, Hong-Joon ; Sagong, Borum...
Genes & Genomics. 38 (2016) 10 - p. 961-966 , 2016

Link: https://doi.org/10.1007/..

5

Screening of the SLC17A8 gene as a causative factor for aut..:

Ryu, Nari ; Sagong, Borum ; Park, Hong-Joon...
BMC Medical Genetics. 17 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

6

Genetic association of MYH genes with hereditary hearing lo..:

Kim, Sang-Joo ; Lee, Seokwon ; Park, Hong-Joon...
Gene. 591 (2016) 1 - p. 177-182 , 2016

Link: https://doi.org/10.1016/..

7

A novel missense variant in the DIAPH1 gene in a Korean fam..:

Kang, Tae-Hun ; Baek, Jeong-In ; Sagong, Borum...
Genes & Genetic Systems. 91 (2016) 5 - p. 289-292 , 2016

Link: https://doi.org/10.1266/..

8

Carrier frequency of SLC26A4 mutations causing inherited de..:

Kim, Hyogyeong ; Lim, Hwan-Sub ; Ryu, Jae-Song...
Journal of Genetic Medicine. 11 (2014) 2 - p. 63-68 , 2014

Link: https://doi.org/10.5734/..

9

Genetic Analysis of Genes Related to Tight Junction Functio..:

Kim, Min-A ; Kim, Ye-Ri ; Sagong, Borum...
PLoS ONE. 9 (2014) 4 - p. e95646 , 2014

Link: https://doi.org/10.1371/..

10

Identification of CDH23 mutations in Korean families with h..:

Woo, Hae-Mi ; Park, Hong-Joon ; Park, Mi-Hyun...
BMC Medical Genetics. 15 (2014) 1 - p. , 2014

Link: https://doi.org/10.1186/..

11

Whole-exome sequencing identifies MYO15A mutations as a cau..:

Woo, Hae-Mi ; Park, Hong-Joon ; Baek, Jeong-In...
BMC Medical Genetics. 14 (2013) 1 - p. , 2013

Link: https://doi.org/10.1186/..

12

A novel synonymous mutation causing complete skipping of ex..:

Kim, Yoonjung ; Kim, Hui Ram ; Kim, Juwon...
Biochemical and Biophysical Research Communications. 430 (2013) 3 - p. 1147-1150 , 2013

Link: https://doi.org/10.1016/..

13

Limitations of hearing screening in newborns with PDS mutat..:

Kim, Bo Gyung ; Shin, Joong-Wook ; Park, Hong-Joon...
International Journal of Pediatric Otorhinolaryngology. 77 (2013) 5 - p. 833-837 , 2013

Link: https://doi.org/10.1016/..

14

Identification and functional characterization of novel com..:

Sagong, Borum ; Park, Hong-Joon ; Lee, Kyu-Yup.
Gene. 492 (2012) 1 - p. 239-243 , 2012

Link: https://doi.org/10.1016/..

15

A novel COCH mutation associated with autosomal dominant no..:

Cho, Hyun-Ju ; Park, Hong-Joon ; Trexler, Maria...
Journal of Molecular Medicine. 90 (2012) 11 - p. 1321-1331 , 2012

Link: https://doi.org/10.1007/..