Search Results - Go Hun Seo

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  1. 1
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    Growth hormone therapy in patients with Noonan syndrome by Go Hun Seo, Han-Wook Yoo

    Published 2018
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  2. 2
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    Growth hormone deficiency in a boy with Wiedemann-Steiner syndrome: a case report and review by Mi Ra Kim, Eun-Gyong Yoo, Seonkyeong Rhie, Go Hun Seo, Mo Kyung Jung

    Published 2022
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  3. 3
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    A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy by Seung Ho Kim, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Jeesuk Yu

    Published 2023
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  4. 4
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    Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report by Dai Jung, Go Hun Seo, Yoon-Myung Kim, Jin-Ho Choi, Han-Wook Yoo

    Published 2018
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  5. 5
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    A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing by Yoon-Myung Kim, Go Hun Seo, Gu-Hwan Kim, Jung Min Ko, Jin-Ho Choi, Han-Wook Yoo

    Published 2018
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  6. 6
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    Turner syndrome presented with tall stature due to overdosage of the gene by Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo

    Published 2015
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  7. 7
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    Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous Mutation by So Jeong Kim, Jeong Eun Lee, Hyun Duck Kwak, Mi Seon Kang, Seong Ah Yu, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung

    Published 2021
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  8. 8
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    Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay by Go Hun Seo, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo

    Published 2016
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  9. 9
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    Genetic heterogeneity of cardiomyopathy and its correlation with patient care by Mi Jin Kim, Seulgi Cha, Jae Suk Baek, Jeong Jin Yu, Go Hun Seo, Minji Kang, Hyo-Sang Do, Sang Eun Lee, Beom Hee Lee

    Published 2023
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  10. 10
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    An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial non-autoimmune hyperthyroidism by Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak

    Published 2020
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  11. 11
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    Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea by Yena Lee, Yunha Choi, Go Hun Seo, Gu-Hwan Kim, Changwon Keum, Yoo-Mi Kim, Hyo-Sang Do, Jeongmin Choi, In Hee Choi, Han-Wook Yoo, Beom Hee Lee

    Published 2021
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  12. 12
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    Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management by Jiwon Jung, Joo Hoon Lee, Young Seo Park, Go Hun Seo, Changwon Keum, Hee Gyung Kang, Hajeong Lee, Sang Koo Lee, Sang Taek Lee, Heeyeon Cho, Beom Hee Lee

    Published 2021
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  13. 13
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    Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay by Go Hun Seo, Hane Lee, Jungsul Lee, Heonjong Han, You Kyung Cho, Minji Kim, Yunha Choi, Jeongmin Choi, In Hee Choi, Seonkyeong Rhie, Kyu Young Chae, Yoo-Mi Kim, Chong Kun Cheon, Su Jin Kim, Jieun Lee, Eungu Kang, Jung Hye Byeon, Hee Joon Yu, Young-Lim Shin, Arum Oh, Woo Jin Kim, Mi-Sun Yum, Beom Hee Lee, Baik-Lin Eun

    Published 2022
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