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[Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis].

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Title: [Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis].
Authors: Mo Y; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China., Xiao FF; Department of Clinical Immunology and Allergy, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China., Wang HJ; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China., Wu BB; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China., Lu Y; Department of Hepatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China., Cheng GQ; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China., Li L; Department of Neonatology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830054, China., Chen DM; Department of Neonatology, Quanzhou Maternity and Children's Hospital, Fujian, Quanzhou 362000, China., Lu YL; Department of Molecular Medical Center, Guangzhou Medical University Affiliated Women and Children's Medical Center, Guangzhou 511436, China., Zhou W; Department of Neonatology, Guangzhou Medical University Affiliated Women and Children's Medical Center, Guangzhou 511436, China., Wei QF; Neonatal Medical Center, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning 530002, China., Zhou WH; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China.
Source: Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2026 Mar 14; Vol. 64 (4), pp. 415-420. Date of Electronic Publication: 2026 Mar 14.
Publication Type: English Abstract; Journal Article
Journal Info: Publisher: Chinese Medical Association Country of Publication: China NLM ID: 0417427 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0578-1310 (Print) Linking ISSN: 05781310 NLM ISO Abbreviation: Zhonghua Er Ke Za Zhi Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: [Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis].
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  Data: <searchLink fieldCode="AU" term="%22Mo+Y%22">Mo Y</searchLink>; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Xiao+FF%22">Xiao FF</searchLink>; Department of Clinical Immunology and Allergy, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Wang+HJ%22">Wang HJ</searchLink>; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Wu+BB%22">Wu BB</searchLink>; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Lu+Y%22">Lu Y</searchLink>; Department of Hepatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Cheng+GQ%22">Cheng GQ</searchLink>; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China.<br /><searchLink fieldCode="AU" term="%22Li+L%22">Li L</searchLink>; Department of Neonatology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830054, China.<br /><searchLink fieldCode="AU" term="%22Chen+DM%22">Chen DM</searchLink>; Department of Neonatology, Quanzhou Maternity and Children's Hospital, Fujian, Quanzhou 362000, China.<br /><searchLink fieldCode="AU" term="%22Lu+YL%22">Lu YL</searchLink>; Department of Molecular Medical Center, Guangzhou Medical University Affiliated Women and Children's Medical Center, Guangzhou 511436, China.<br /><searchLink fieldCode="AU" term="%22Zhou+W%22">Zhou W</searchLink>; Department of Neonatology, Guangzhou Medical University Affiliated Women and Children's Medical Center, Guangzhou 511436, China.<br /><searchLink fieldCode="AU" term="%22Wei+QF%22">Wei QF</searchLink>; Neonatal Medical Center, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning 530002, China.<br /><searchLink fieldCode="AU" term="%22Zhou+WH%22">Zhou WH</searchLink>; Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defects, National Children's Medical Center, Shanghai 201102, China.
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  Data: <searchLink fieldCode="JN" term="%220417427%22">Zhonghua er ke za zhi = Chinese journal of pediatrics</searchLink> [Zhonghua Er Ke Za Zhi] 2026 Mar 14; Vol. 64 (4), pp. 415-420. <i>Date of Electronic Publication: </i>2026 Mar 14.
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  Data: English Abstract; Journal Article
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Chinese+Medical+Association%22">Chinese Medical Association </searchLink><i>Country of Publication: </i>China <i>NLM ID: </i>0417427 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0578-1310 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2205781310%22">05781310 </searchLink><i>NLM ISO Abbreviation: </i>Zhonghua Er Ke Za Zhi <i>Subsets: </i>MEDLINE
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        Value: 10.3760/cma.j.cn112140-20251031-00970
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      – Code: chi
        Text: Chinese
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              Text: 2026 Mar 14
              Type: published
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