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Showing page 1 of results 1 - 10 of about 67 pages

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Insulin Resistance Leads to Mitochondrial Dysfunction in Hepatocyte | ESPE2019
Hong Chen; Yanlan Fang; Li Liang; Chunlin Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092FC1.1
Published: 2019-08-22

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Insulin Resistance Leads to Mitochondrial Dysfunction in Hepatocyte | ESPE2019
Hong Chen; Yanlan Fang; Li Liang; Chunlin Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092fc1.1.html
Published: 2019-08-22

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A Novel Compound Heterozygous Mutation of the CYP17A1 Gene is Associated with Rhabdomyolysis: Demonstration of Combining 17[alpha]-hydroxylase/17,20-Lyase Deficiency | ESPE2018
Hong Chen; Chunlin Wang; Li Liang; Qingfeng Yan
http://abstracts.eurospe.org/hrp/0089/hrp0089lb-p15.htm
Published: 2018-08-28

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A Novel MAP3K1 Gene Mutation (c.556A>G) Associated with 46, XY Complete Gonadal Dysgenesis | ESPE2019
Yilin Zhu; Hong Chen; Minfei He; Li Liang; Chunlin Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-278
Published: 2019-08-22

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A Novel MAP3K1 Gene Mutation (c.556A>G) Associated with 46, XY Complete Gonadal Dysgenesis | ESPE2019
Yilin Zhu; Hong Chen; Minfei He; Li Liang; Chunlin Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-278.html
Published: 2019-08-22

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8 hit(s)
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Family Investigation and Clinical Phenotype Analysis of Type A Insulin Resistance Syndrome | ESPE2018
Yonghua Chen; Hong Chen; Yanlan Fang; Chunlin Wang; Jianfang Zhu; Li Liang
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p399.htm
Published: 2018-08-28

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A Novel Compound Heterozygous Mutation in the CYP11B2 Gene, Including an Intron 7 Splice Site, is Responsible for Aldosterone Synthase Deficiency Type II | ESPE2019
Jianfang Zhu; Hong Chen; Chunlin Wang; Yanlan Fang; Yuanmei Kong; Li Liang
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-297
Published: 2019-08-22

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8 hit(s)
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A Novel Compound Heterozygous Mutation in the CYP11B2 Gene, Including an Intron 7 Splice Site, is Responsible for Aldosterone Synthase Deficiency Type II | ESPE2019
Jianfang Zhu; Hong Chen; Chunlin Wang; Yanlan Fang; Yuanmei Kong; Li Liang
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-297.html
Published: 2019-08-22

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Indentification of a de Novo Mutation in the SRY Gene in a 46,XY Complete Gonadal Dysgenesis Patient with Gonadal Neoplasia and Review of Tumor Risk in 46,XY DSD Patients | ESPE2019
Minfei He; Hong Chen; Yilin Zhu; Yanlan Fang; Jianfang Zhu; Li Liang; Chunling Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-223
Published: 2019-08-22

68% match
8 hit(s)
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Indentification of a de Novo Mutation in the SRY Gene in a 46,XY Complete Gonadal Dysgenesis Patient with Gonadal Neoplasia and Review of Tumor Risk in 46,XY DSD Patients | ESPE2019
Minfei He; Hong Chen; Yilin Zhu; Yanlan Fang; Jianfang Zhu; Li Liang; Chunling Wang
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-223.html
Published: 2019-08-22

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