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A Case of Permanent Congenital Hypothyroidism with Compound Heterozygous Mutations in the DUOX2 Gene | ESPE2018
Jeongju Hwang; Ja-Hyun Jang; Jeesuk Yu
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p380.htm
Published: 2018-08-28

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Targeted Exome Sequencing for Genetic Diagnosis of Patients with Disorders of Sex Development | ESPE2016
Ja Hye Kim; Eungu Kang; Gu-Hwan Kim; Ja-Hyun Jang; Eun-Hae Cho; Beom Hee Lee; Han-Wook Yoo; Jin-Ho Choi
http://abstracts.eurospe.org/hrp/0086/hrp0086fc7.5.htm
Published: 2016-08-19

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