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Manifestation of Giant Bilateral Symptomatic Adrenal Myelolipomas in an Adult Patient with Congenital Adrenal Hyperplasia.
Yoo Mi Kim, Jin Ho Choi, Beom Hee Lee, Gu Hwan Kim, Beom Sik Hong, Yong Jun Ryu, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2012;17(4):244-248.
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A Familial Case of Kallmann Syndrome due to KAL1 Gene Complete Deletion.
Sun Hee Lee, Seong Woo Han, Gu Hwan Kim, Han Wook Yoo, Woo Yeong Chung
Ann Pediatr Endocrinol Metab. 2011;16(1):61-65.
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A Novel Mutation of the Steroid 5-Alpha Reductase Type 2 (SRD5A2) Gene in a Korean Newborn with Ambiguous Genitalia.
Ran Hee Kim, Su Yung Kim, Han Wook Yoo, Gu Hwan Kim, Chong Kun Cheon
Ann Pediatr Endocrinol Metab. 2010;15(2):133-137.
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A Case of Hyperinsulinism/Hyperammonemia (HI/HA) Syndrome due to a Mutation in the Glutamate Dehydrogenase Gene (GLUD1).
Hye Young Jin, Jin Ho Choi, Gu Hwan Kim, Jung Min Ko, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2009;14(2):168-173.
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Molecular Genetic Analysis and Endocriological Evaluation of Isolated Hypogonadotropic Hypogonadism Presented with Delayed Puberty.
Jung Min Ko, Gu Hwan Kim, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2007;12(1):41-48.
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Clinical Manifestation and Effect of Corn Starch on Height Growth in Korean Patients with Glycogen Storage Disease Type Ia.
Jungi Choi, Jung Min Ko, Gu Hwan Kim, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2007;12(1):35-40.
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Genotype of Steroid 21-Hydroxylase Gene and Clinical Characteristics in Patients with Congenital Adrenal Hyperplasia 21-Hydroxylase Deficiency.
Jung Min Ko, Jin Ho Choi, Gu Hwan Kim, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2005;10(1):57-63.
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