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Shaoke Chen

Showing results (21-30 of 80) with videos related to

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Molecular Cytogenetics|February 5, 2015
Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)Rongyu Chen, Chuan Li, Bobo Xie, et al.
Gene|February 16, 2016
Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern ChinaSheng He, Qian Qin, Shang Yi, et al.
Gene|December 3, 2015
Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposisShujie Zhang, Haisong Qin, Weigang Lv, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 21, 2019
Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorderFei Chen, Haiming Yuan, Wenyong Wu, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
BMC Pediatrics|August 1, 2019
U-shaped relationship between birth weight and childhood blood pressure in ChinaChong Lai, Yiyan Hu, Di He, et al.
Genetics Research|August 4, 2025
49, XXXYY: Parental Origin, Occurrence, and Clinical PhenotypesYufang Du, Liangrong Liao, Xianda Wei, et al.
Molecular Cytogenetics|June 2, 2016
A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic featuresBobo Xie, Xin Fan, Yaqin Lei, et al.
Molecular Cytogenetics|May 10, 2016
de novo interstitial deletions at the 11q23.3-q24.2 regionJiasun Su, Rongyu Chen, Jingsi Luo, et al.
Frontiers in Pharmacology|April 2, 2019
Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter StudyXiu Zhao, Yanning Song, Shaoke Chen, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Molecular Cytogenetics|February 5, 2015
Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)Rongyu Chen, Chuan Li, Bobo Xie, et al.
Gene|February 16, 2016
Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern ChinaSheng He, Qian Qin, Shang Yi, et al.
Gene|December 3, 2015
Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposisShujie Zhang, Haisong Qin, Weigang Lv, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 21, 2019
Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorderFei Chen, Haiming Yuan, Wenyong Wu, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
BMC Pediatrics|August 1, 2019
U-shaped relationship between birth weight and childhood blood pressure in ChinaChong Lai, Yiyan Hu, Di He, et al.
Genetics Research|August 4, 2025
49, XXXYY: Parental Origin, Occurrence, and Clinical PhenotypesYufang Du, Liangrong Liao, Xianda Wei, et al.
Molecular Cytogenetics|June 2, 2016
A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic featuresBobo Xie, Xin Fan, Yaqin Lei, et al.
Molecular Cytogenetics|May 10, 2016
de novo interstitial deletions at the 11q23.3-q24.2 regionJiasun Su, Rongyu Chen, Jingsi Luo, et al.
Frontiers in Pharmacology|April 2, 2019
Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter StudyXiu Zhao, Yanning Song, Shaoke Chen, et al.
Pageof 8