ESPE Abstracts Search

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Showing page 1 of results 1 - 10 of about 17 pages

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Vitamin D Dependent Rickets Type 1A with Genetic Analysis in Three Chinese Children | ESPE2015
Wenjing Li; Chunxiu Gong; Liya Wei
http://abstracts.eurospe.org/hrp/0084/hrp0084p3-647.htm
Published: 2015-08-26

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A Novel Heterozygous Pathogenic Variant in PORCN Gene Causing Focal Dermal Hypoplasia with Short Stature: Case Report and Literature Review | ESPE2018
Di Wu; Xuyun Hu; Xiaoqiao Li; Liya Wei; Chang Su; Jiajia Chen; Miao Qin; Chunxiu Gong; Yiping Shen
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p229.htm
Published: 2018-08-28

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Study of GH Receptor exon 3 Polymorphism in Children With Prader-Willi Syndrome | ESPE2014
Feihong Luo; Wei Lu; Zhou Pei; Zhangqian Zheng
http://abstracts.eurospe.org/hrp/0082/hrp0082p3-d1-821.htm
Published: 2014-08-28

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Mutation of RET Gene Causes Multiple Endocrine Neoplasia Type 2B in an Adolescent: Report of One Case and Literature Review | ESPE2019
Lidan Zhang; Yan Guo; Lei Ye; Zhiya Dong; Wenli Lu; Wei Wang; Yuan Xiao
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-261
Published: 2019-08-22

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Central Precocious Puberty in a boy with Prader-Willi Syndromeduring Growth Hormone Replacement Therapy | ESPE2019
WEI LU; Zhangqian Zheng; Jinwen Ni; Xiaojing Li; Li Xi; Feihong Luo
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-197
Published: 2019-08-22

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A Chinese Girl Suffered Both Osteogenesis Imperfecta and Mucopolysaccharidosis: Trio WES Could Tell us More | ESPE2019
Zhangqian Zheng; Lin Yang; Wei Lu; Feihong Luo
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-32
Published: 2019-08-22

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