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Author/Creator Kim, Hyung-Goo

2. Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish. Issue 5 (30th January 2021)

Authors:
Lee, Yu-Ri; Kim, Se Hee; Ben-Mahmoud, Afif; Kim, Oc-Hee; Choi, Tae-Ik; Lee, Kang-Han; Ku, Bonsu; Eum, Juneyong; Kee, Yun; Lee, Sangkyu; Cha, Jihoon; Won, DongJu; Lee, Seung-Tae; Choi, Jong Rak; Lee, Joon Soo; Kim, Heung Dong; Kim, Hyung-Goo; Bonkowsky, Joshua L; Kang, Hoon-Chul; Kim, Cheol-Hee
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 5(2021)
Page Start:
331
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome. (5th December 2016)

Authors:
Quaynor, Samuel D.; Bosley, Maggie E.; Duckworth, Christina G.; Porter, Kelsey R.; Kim, Soo-Hyun; Kim, Hyung-Goo; Chorich, Lynn P.; Sullivan, Megan E.; Choi, Jeong-Hyeon; Cameron, Richard S.; Layman, Lawrence C.
Journal:
Molecular and cellular endocrinology
Issue:
Volume 437(2016)
Page Start:
86
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome. (5th December 2016)

Authors:
Quaynor, Samuel D.; Bosley, Maggie E.; Duckworth, Christina G.; Porter, Kelsey R.; Kim, Soo-Hyun; Kim, Hyung-Goo; Chorich, Lynn P.; Sullivan, Megan E.; Choi, Jeong-Hyeon; Cameron, Richard S.; Layman, Lawrence C.
Journal:
Molecular and cellular endocrinology
Issue:
Volume 437(2016)
Page Start:
86
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗