Results
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Persistent and energetic bottom-trapped topographic Rossby waves observed in the southern South China Sea. [electronic resource] by
- Shu, Yeqiang
- Xue, Huijie
- Wang, Dongxiao
- Chai, Fei
- Xie, Qiang
- Cai, Shuqun
- Chen, Rongyu
- Chen, Ju
- Li, Jian
- He, Yunkai
Producer: 20161213
In:
Scientific reports vol. 6
Availability: No items available.
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12.
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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
Availability: No items available.
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13.
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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
Availability: No items available.
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14.
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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
Availability: No items available.
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15.
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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
Availability: No items available.
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16.
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[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
Availability: No items available.
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17.
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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
Availability: No items available.
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18.
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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
Availability: No items available.
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19.
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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
Availability: No items available.
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20.
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A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33. [electronic resource] by
- Wang, Jin
- Fu, Chunyun
- Zhang, Shujie
- Luo, Jingsi
- Ouyang, Luping
- Xie, Bobo
- Sun, Weijia
- He, Sheng
- Su, Jiasun
- Hu, Xuyun
- Fei, Dongmei
- Chen, Rongyu
- Fan, Xin
- Ou, Shan
- Chen, Shaoke
- Shen, Yiping
Producer: 20170126
In:
Gene vol. 594
Availability: No items available.
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