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	1.	Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism. [electronic resource] by Fu, Chunyun Chen, Shaoke Chen, Rongyu Fan, Xin Luo, Jingsi Li, Chuan Qian, Jiale Producer: 20150622 In: Arquivos brasileiros de endocrinologia e metabologia vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Gene distribution characteristics of deletional α-thalassemia in Guangxi region]. [electronic resource] by Zhang, Qiang Fan, Xin He, Sheng Fu, Chunyun Tang, Yanqing Chen, Qiuli Wei, Yuan Zheng, Chenguang Producer: 20150516 In: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Genotypes of 1 571 cases of Hb H disease in Guangxi area]. [electronic resource] by Fu, Chunyun Chen, Shaoke Zhang, Qiang He, Sheng Wei, Yuan Chen, Qiuli Tang, Yanqing Zheng, Chenguang Producer: 20150105 In: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	State Transition for Statistical SLAM Using Planar Features in 3D Point Clouds. [electronic resource] by Gostar, Amirali Khodadadian Fu, Chunyun Chuah, Weiqin Hossain, Mohammed Imran Tennakoon, Ruwan Bab-Hadiashar, Alireza Hoseinnezhad, Reza Publication details: Sensors (Basel, Switzerland) Apr 2019 In: Sensors (Basel, Switzerland) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Tetravalent recombinant dengue virus-like particles as potential vaccine candidates: immunological properties. [electronic resource] by Liu, Yan Zhou, Junmei Yu, Zhizhun Fang, Danyun Fu, Chunyun Zhu, Xun He, Zhenjian Yan, Huijun Jiang, Lifang Producer: 20151012 In: BMC microbiology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Genetic testing and pregnancy outcome of 337 fetuses with urinary system anomalies]. [electronic resource] by Zeng, Shangjuan Wang, Lifang Luo, Shiyu Li, Qifei Qiu, Xiaoxia Gui, Chunrong Liu, Tiansheng Wei, Hongwei Ma, Gang Fu, Chunyun Producer: 20190820 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound. [electronic resource] by Luo, Shiyu Meng, Dahua Li, Qifei Hu, Xuehua Chen, Yuhua He, Chun Xie, Bobo She, Shangyang Li, Yingfeng Fu, Chunyun Producer: 20190207 In: Arquivos brasileiros de cardiologia vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis. [electronic resource] by Zhang, Shujie Qin, Haisong Lv, Weigang Luo, Shiyu Wang, Jin Fu, Chunyun Ma, Ruiyu Shen, Yiping Chen, Shaoke Wu, Lingqian Producer: 20160617 In: Gene vol. 577 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Skp2 regulates subcellular localization of PPARγ by MEK signaling pathways in human breast cancer. [electronic resource] by Cheng, Hongge Meng, Jie Wang, Guisheng Meng, Yuming Li, Yu Wei, Dong Fu, Chunyun Deng, Kaifeng Shen, Aiguo Wang, Huimin Dai, Shengming Producer: 20140407 In: International journal of molecular sciences vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	de novo interstitial deletions at the 11q23.3-q24.2 region. [electronic resource] by Su, Jiasun Chen, Rongyu Luo, Jingsi Fan, Xin Fu, Chunyun Wang, Jin He, Sheng Hu, Xuyun Zhang, ShuJie Yi, Shang Chen, Shaoke Shen, Yiping Producer: 20160509 In: Molecular cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mosaic UPD(7q)mat in a patient with silver Russell syndrome. [electronic resource] by Su, Jiasun Wang, Jin Fan, Xin Fu, Chunyun Zhang, ShuJie Zhang, Yue Qin, Zailong Li, Hongdou Luo, Jingsi Li, Chuan Jiang, Tingting Shen, Yiping Publication details: Molecular cytogenetics 2017 In: Molecular cytogenetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features. [electronic resource] by Xie, Bobo Fan, Xin Lei, Yaqin Chen, Rongyu Wang, Jin Fu, Chunyun Yi, Shang Luo, Jingsi Zhang, Shujie Yang, Qi Chen, Shaoke Shen, Yiping Producer: 20160601 In: Molecular cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism. [electronic resource] by Fan, Xin Fu, Chunyun Shen, Yiping Li, Chuan Luo, Shiyu Li, Qifei Luo, Jingsi Su, Jiasun Zhang, Shujie Hu, Xuyun Chen, Rongyu Gu, Xuefan Chen, Shaoke Producer: 20180110 In: Clinica chimica acta; international journal of clinical chemistry vol. 468 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation]. [electronic resource] by Luo, Shiyu Fu, Chunyun Zhang, Shujie Wang, Jin Fan, Xin Luo, Jingsi Chen, Rongyu Hu, Xuyun Qin, Haisong Li, Chuan Ou, Shan Li, Qifei Chen, Shaoke Producer: 20170914 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. [electronic resource] by Zhang, Shujie Qin, Haisong Wang, Jin OuYang, Luping Luo, Shiyu Fu, Chunyun Fan, Xin Su, Jiasun Chen, Rongyu Xie, Bobo Hu, Xuyun Chen, Shaoke Shen, Yiping Producer: 20160825 In: Molecular cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism. [electronic resource] by Fu, Chunyun Xie, Bobo Zhang, Shujie Wang, Jin Luo, Shiyu Zheng, Haiyang Su, Jiasun Hu, Xuyun Chen, Rongyu Fan, Xin Luo, Jingsi Gu, Xuefan Chen, Shaoke Producer: 20171206 In: BMJ open vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations. [electronic resource] by Fu, Chunyun Luo, Shiyu Zhang, Yue Fan, Xin D'Gama, Alissa M Zhang, Xiaofei Zheng, Haiyang Su, Jiasun Li, Chuan Luo, Jingsi Agrawal, Pankaj B Li, Qifei Chen, Shaoke Producer: 20190318 In: Clinica chimica acta; international journal of clinical chemistry vol. 489 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates. [electronic resource] by Fu, Chunyun Luo, Shiyu Li, Qifei Xie, Bobo Yang, Qi Geng, Guoxing Lin, Caijuan Su, Jiasun Zhang, Yue Wang, Jin Qin, Zailong Luo, Jingsi Chen, Shaoke Fan, Xin Producer: 20181119 In: Scientific reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism. [electronic resource] by Fu, Chunyun Zheng, Haiyang Zhang, Shujie Chen, Yun Su, Jiasun Wang, Jin Xie, Bobo Hu, Xuyun Fan, Xin Luo, Jingsi Li, Chuan Chen, Rongyu Shen, Yiping Chen, Shaoke Producer: 20170628 In: Archives of endocrinology and metabolism vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients. [electronic resource] by Fu, Chunyun Luo, Shiyu Zhang, Shujie Wang, Jin Zheng, Haiyang Yang, Qi Xie, Bobo Hu, Xuyun Fan, Xin Luo, Jingsi Chen, Rongyu Su, Jiasun Shen, Yiping Gu, Xuefan Chen, Shaoke Producer: 20170203 In: Clinica chimica acta; international journal of clinical chemistry vol. 458 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 27 results.