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Clinical Genetics|October 23, 2023
The third case of Marbach-Rustad progeroid syndrome caused by a de novo LEMD2 variantZhikun Lu, Wen Zhang, Xiaojian Mao, et al.
European Journal of Immunology|February 6, 2018
Somatic and germline FOXP3 mosaicism in the mother of a boy with IPEX syndromeYunting Lin, Aijing Xu, Chunhua Zeng, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|February 28, 2024
Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel <i>PLCB4</i> Splicing Variant and 5-Year Follow-upYunting Lin, Ye Zhang, Jian Ma, et al.
European Journal of Endocrinology|October 29, 2019
'Isolated' germline mosaicism in the phenotypically normal father of a girl with X-linked hypophosphatemic ricketsYunting Lin, Yanna Cai, Jianan Xu, et al.
Medicine|April 6, 2018
Pediatric hyperimmunoglobulin E syndrome: A case series of 4 children in ChinaHuifeng Fan, Li Huang, Diyuan Yang, et al.
The American Journal of Sports Medicine|July 22, 2022
Comparative Effects of Exosomes and Ectosomes Isolated From Adipose-Derived Mesenchymal Stem Cells on Achilles Tendinopathy in a Rat ModelTengjing Xu, Yunting Lin, Xinning Yu, et al.
Calcified Tissue International|September 6, 2021
Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic RicketsYunting Lin, Wen Zhang, Xinjiang Huang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 21, 2019
Clinical and molecular characteristics of carnitine-acylcarnitine translocase deficiency: Experience with six patients in Guangdong ChinaChengfang Tang, Sichi Liu, Meigui Wu, et al.
Journal of Clinical Lipidology|February 21, 2019
Clinical features, molecular characteristics, and treatments of a Chinese girl with sitosterolemia: A case report and literature reviewXueying Su, Yongxian Shao, Yunting Lin, et al.
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