Phenotypes of Cornelia de Lange syndrome caused by non-cohesion genes: Novel variants and literature review by Shangguan, Huakun, Chen, Ruimin

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Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature by Shangguan, Huakun, Su, Chang, Ouyang, Qian, Cao, Bingyan, Wang, Jian, Gong, Chunxiu, Chen, Ruimin

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The clinical and genetic aspects of six individuals with GH1 variants and isolated growth hormone deficiency type II by Huang, Xiaozhen, Chen, Hong, Shangguan, Huakun, Wu, Wenyong, Ai, Zhuanzhuan, Chen, Zhifeng, Chen, Ruimin

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Clinical and genetic analysis of two Chinese families with vitamin D-dependent rickets type IA and follow-up by Li, Yunfei, Yuan, Xin, Chen, Ruimin, Lin, Xiangquan, Shangguan, Huakun, Yang, Xiaohong, Zhang, Ying

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Associations of Obesity With Growth and Puberty in Children: A Cross-Sectional Study in Fuzhou, China by Zhang, Ying, Yuan, Xin, Yang, XiaoHong, Lin, XiangQuan, Cai, ChunYan, Chen, ShiJun, Ai, ZhuanZhuan, ShangGuan, HuaKun, Wu, WenYong, Chen, RuiMin

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Intervention Effect of Probiotics on the Early Onset of Puberty Induced by Daidzein in Female Mice by Yuan, Xin, Shangguan, Huakun, Zhang, Ying, Lin, Xiangquan, Chen, Ruimin

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Knockdown of Kmt2d leads to growth impairment by activating the Akt/β-catenin signaling pathway by Shangguan, Huakun, Huang, Xiaozhen, Lin, Jinduan, Chen, Ruimin

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A study on genotypes and phenotypes of short stature caused by epigenetic modification gene variants by Shangguan, Huakun, Wang, Jian, Lin, Jinduan, Huang, Xiaozhen, Zeng, Yan, Chen, Ruimin

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Clinical features, genetic detection and therapeutic response to rhGH of children with Noonan syndrome: an analysis of 12 cases by Shangguan, Huakun, Xu, Yuanbin, Chen, Ruimin

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12例努南综合征患儿的临床特征及重组人生长激素疗效观察 by SHANGGUAN, Huakun, XU, Yuanbin, CHEN, Ruimin

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12例努南综合征患儿的临床特征及重组人生长激素疗效观察 by 上官华坤, 徐源彬, 陈瑞敏

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