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Personalized Medicine Volume 18, 2021 - Issue 6
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Short Communication

miR-938rs2505901 T>C Polymorphism Increases Hirschsprung Disease Risk: A Case–Control Study of Chinese Children

Jun Zhong1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaView further author information
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Jiabin Liu1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaView further author information
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Yi Zheng1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaView further author information
,
Xiaoli Xie1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaView further author information
,
Qiuming He1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaView further author information
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Wei Zhong1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-0637-3743View further author information
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Qiang Wu1 Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women & Children’s Medical Center, Guangzhou Medical University, Guangzhou510623, Guangdong, ChinaCorrespondence[email protected]
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Pages 551-558 | Received 05 Jan 2021, Accepted 25 Aug 2021, Published online: 11 Nov 2021

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