Hasil Pencarian - Chunxiu Gong
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Editorial: Childhood Diabetes in Low- and Middle-Income Countries oleh Chunxiu Gong
Diterbitkan 2022-01-01Dapatkan teks lengkap
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Phenotype and Molecular Characterizations of 30 Children From China With NR5A1 Mutations oleh Yanning Song, Lijun Fan, Chunxiu Gong, Chunxiu Gong
Diterbitkan 2018-10-01Dapatkan teks lengkap
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Central precocious puberty as a prelude to hypogonadism in a patient with Klinefelter syndrome oleh Chunxiu Gong, Lele Li, Jiahui Chen, Wenjing Li
Diterbitkan 2019-06-01Dapatkan teks lengkap
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Sifrim–Hitz‐Weiss/CHD4‐related syndrome: A new case report oleh Beibei Zhang, Ming Cheng, Lijun Fan, Chunxiu Gong
Diterbitkan 2023-06-01Dapatkan teks lengkap
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Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency oleh Ying Liu, Lijun Fan, Xiaoling Wang, Chunxiu Gong
Diterbitkan 2021-12-01Dapatkan teks lengkap
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Analysis in the influence factors of urethroplasty in DSD oleh Jing Yu, Ning Sun, Hongcheng Song, Minglei Li, Lele Li, Chunxiu Gong, Weiping Zhang
Diterbitkan 2022-08-01Dapatkan teks lengkap
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Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature oleh Huakun Shangguan, Chang Su, Qian Ouyang, Bingyan Cao, Jian Wang, Chunxiu Gong, Ruimin Chen
Diterbitkan 2019-11-01Dapatkan teks lengkap
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Validity of web‐based self‐assessment of pubertal development against pediatrician assessments oleh Xiaoxia Peng, Yaguang Peng, Yuchuan Li, Xiaolu Nie, Chunxiu Gong, Di Wu, Xin Ni
Diterbitkan 2018-09-01Dapatkan teks lengkap
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SOX2 heterozygous mutations cause multiple extraocular phenotypes in boys oleh Yi Wang, Lijun Fan, Xiaoya Ren, Yanning Song, Beibei Zhang, Chunxiu Gong, Peifang Wei
Diterbitkan 2022-02-01Dapatkan teks lengkap
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Clinical characteristics and genotype‐phenotype correlations of 130 Chinese children in a high‐homogeneity single‐center cohort with 5α‐reductase 2 deficiency oleh Lijun Fan, Yanning Song, Michel Polak, Lele Li, Xiaoya Ren, Beibei Zhang, Di Wu, Chunxiu Gong
Diterbitkan 2020-10-01Dapatkan teks lengkap
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Clinical, Biochemical, Molecular, and Outcome Features of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency in 10 Chinese Patients oleh Shengnan Wu, Linghua Shen, Qiong Chen, Chunxiu Gong, Yanling Yang, Haiyan Wei, Bingyan Cao, Yongxing Chen
Diterbitkan 2022-03-01Dapatkan teks lengkap
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Correction to: One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria oleh Liping Hou, Ming Zhao, Lijun Fan, Bingyan Cao, Jiajia Chen, Yonghua Cui, Michel Polak, Chunxiu Gong
Diterbitkan 2022-03-01Dapatkan teks lengkap
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Clinical and genetic characteristics of hypophosphatasia in Chinese children oleh Meijuan Liu, Min Liu, Xuejun Liang, Di Wu, Wenjing Li, Chang Su, Bingyan Cao, Jiajia Chen, Chunxiu Gong
Diterbitkan 2021-04-01Dapatkan teks lengkap
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