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Risk Management and Healthcare Policy Volume 14, 2021 - Issue
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Original Research

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study

Hailong Huang1 Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou City, Fujian Province, 350001, People’s Republic of ChinaORCID Iconhttps://orcid.org/0000-0003-2924-399XView further author information
ORCID Icon,
Meiying Cai1 Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou City, Fujian Province, 350001, People’s Republic of ChinaORCID Iconhttps://orcid.org/0000-0002-7431-2475View further author information
ORCID Icon,
Wei Ma1 Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou City, Fujian Province, 350001, People’s Republic of China;2 School of Clinical Medicine, Fujian Medical University, Fuzhou City, Fujian Province, 350122, People’s Republic of ChinaView further author information
,
Na Lin1 Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou City, Fujian Province, 350001, People’s Republic of ChinaView further author information
&
Liangpu Xu1 Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou City, Fujian Province, 350001, People’s Republic of ChinaCorrespondence[email protected] [email protected]
ORCID Iconhttps://orcid.org/0000-0001-8815-2735View further author information
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Pages 1533-1540 | Published online: 14 Apr 2021

Citations (4)

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Read on this site (1)

Xiaomei Shi, Jian Lu, Ling Li, Ran Wei & Jing Wu. (2022) Prenatal chromosomal microarray analysis in foetuses with isolated absent or hypoplastic nasal bone. Annals of Medicine 54:1, pages 1297-1302.
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Articles from other publishers (3)

Lei Pan, Hui Liang, Zhuo Meng, Jun Wang, Rui Zhang & Yong Wu. (2022) Assessing the value of second-trimester nasal bone hypoplasia in predicting chromosomal abnormalities: a retrospective chromosomal microarray analysis of 351 fetuses. Archives of Gynecology and Obstetrics 308:4, pages 1263-1270.
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Hanna Moczulska, Marcin Serafin, Katarzyna Wojda, Maciej Borowiec & Piotr Sieroszewski. (2022) Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes. Journal of Clinical Medicine 11:6, pages 1513.
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Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Enrica Marchionni, Alice Traversa & Antonio Pizzuti. (2022) Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis. Diagnostics 12:3, pages 575.
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