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Refined by: language: Chinese remove subject: Prenatal Diagnosis remove
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1
Non-Invasive Prenatal Testing:Results in 3733 Cases of Twin Pregnancy and Association With Factors Such as Age
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Non-Invasive Prenatal Testing:Results in 3733 Cases of Twin Pregnancy and Association With Factors Such as Age

Zhōngguó yīxué kēxuéyuàn xuébào, 2023-12, Vol.45 (6), p.912 [Peer Reviewed Journal]

ISSN: 1000-503X ;DOI: 10.3881/j.issn.1000-503X.15704 ;PMID: 38173101

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2
Prenatal ultrasound features and genetic analysis for 17q12 microdeletion syndrome
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Prenatal ultrasound features and genetic analysis for 17q12 microdeletion syndrome

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2021-12, Vol.46 (12), p.1370

ISSN: 1672-7347 ;DOI: 10.11817/j.issn.1672-7347.2021.210412 ;PMID: 35232906

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3
Clinical application of non-invasive prenatal testing for twin pregnancies
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Clinical application of non-invasive prenatal testing for twin pregnancies

Zhonghua yi xue yi chuan xue za zhi, 2024-01, Vol.41 (1), p.14

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20230505-00263 ;PMID: 38171553

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4
Impact of confined placental mosaicism on non-invasive prenatal testing and pregnancy outcomes
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Impact of confined placental mosaicism on non-invasive prenatal testing and pregnancy outcomes

Zhonghua yi xue yi chuan xue za zhi, 2021-04, Vol.38 (4), p.335

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20200803-00574 ;PMID: 33834459

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5
Analysis of clinical characteristics of discordant structural malformations in one of monochorionic diamnionic twins
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Analysis of clinical characteristics of discordant structural malformations in one of monochorionic diamnionic twins

Chung-hua fu chʿan kʿo tsa chih, 2019-02, Vol.54 (2), p.87

ISSN: 0529-567X ;DOI: 10.3760/cma.j.issn.0529-567x.2019.02.003 ;PMID: 30803166

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6
Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area
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Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area

Zhongguo shi yan xue ye xue za zhi, 2019-12, Vol.27 (6), p.1938

ISSN: 1009-2137 ;DOI: 10.19746/j.cnki.issn.1009-2137.2019.06.037 ;PMID: 31839063

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7
Chromosomal abnormalities and neurological outcomes in fetal cerebral ventriculomegaly: a retrospective cohort analysis
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Chromosomal abnormalities and neurological outcomes in fetal cerebral ventriculomegaly: a retrospective cohort analysis

Hong Kong medical journal = Xianggang yi xue za zhi, 2021-12, Vol.27 (6), p.428-436 [Peer Reviewed Journal]

2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1024-2708 ;EISSN: 2226-8707 ;DOI: 10.12809/hkmj208850 ;PMID: 34949731

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8
Results of non-invasive prenatal testing for 2473 women with twin pregnancy
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Results of non-invasive prenatal testing for 2473 women with twin pregnancy

Zhonghua yi xue yi chuan xue za zhi, 2021-04, Vol.38 (4), p.313

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20200521-00368 ;PMID: 33834454

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9
Correlation of a disintegrin and metalloprotease 12 level in maternal serum during the first trimester with pregnancy outcome
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Correlation of a disintegrin and metalloprotease 12 level in maternal serum during the first trimester with pregnancy outcome

Chung-hua fu chʿan kʿo tsa chih, 2009-06, Vol.44 (6), p.401

ISSN: 0529-567X ;PMID: 19953936

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10
Relationship between sonographic markers and fetal chromosome abnormality during 16-18 weeks of pregnancy
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Article
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Relationship between sonographic markers and fetal chromosome abnormality during 16-18 weeks of pregnancy

Zhong hua yi xue za zhi, 2018-11, Vol.98 (41), p.3320

ISSN: 0376-2491 ;DOI: 10.3760/cma.j.issn.0376-2491.2018.41.005 ;PMID: 30440120

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11
Analysis of genome-wide copy number variations among fetuses with abnormalities detected by prenatal ultrasouography
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Analysis of genome-wide copy number variations among fetuses with abnormalities detected by prenatal ultrasouography

Zhonghua yi xue yi chuan xue za zhi, 2017-04, Vol.34 (2), p.178

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.issn.1003-9406.2017.02.005 ;PMID: 28397213

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12
Prenatal ultrasonographic manifestations and genetic diagnosis of nine fetuses with 7q11.23 duplication syndrome
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Prenatal ultrasonographic manifestations and genetic diagnosis of nine fetuses with 7q11.23 duplication syndrome

Zhonghua yi xue yi chuan xue za zhi, 2024-03, Vol.41 (3), p.266

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20221117-00795 ;PMID: 38448012

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13
Application of whole exome sequencing for the inferential analysis of recessive genetic disease carrier status for couples with a child died of Primary immunodeficiency
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Application of whole exome sequencing for the inferential analysis of recessive genetic disease carrier status for couples with a child died of Primary immunodeficiency

Zhonghua yi xue yi chuan xue za zhi, 2024-02, Vol.41 (2), p.134

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20221220-00879 ;PMID: 38311549

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14
Analysis for the pregnancy outcome of cystic hygroma fetuses and correlation with increased nuchal translucency in first trimester
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Analysis for the pregnancy outcome of cystic hygroma fetuses and correlation with increased nuchal translucency in first trimester

Chung-hua fu chʿan kʿo tsa chih, 2018-10, Vol.53 (10), p.665

ISSN: 0529-567X ;DOI: 10.3760/cma.j.issn.0529-567x.2018.10.003 ;PMID: 30369121

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15
Whole exome sequencing analysis and prenatal diagnosis in children with neurodevelopmental disorders
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Whole exome sequencing analysis and prenatal diagnosis in children with neurodevelopmental disorders

Zhōnghuá yùfáng-yīxué zázhì, 2023-05, Vol.57 (5), p.753

ISSN: 0253-9624 ;DOI: 10.3760/cma.j.cn112150-20220606-00577 ;PMID: 37165823

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16
Prenatal diagnosis of two fetuses with Xp22.31 microdeletion syndrome indicated by non-invasive prenatal testing
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Prenatal diagnosis of two fetuses with Xp22.31 microdeletion syndrome indicated by non-invasive prenatal testing

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.928

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20220825-00576 ;PMID: 37532490

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17
Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome
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Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome

Zhonghua yi xue yi chuan xue za zhi, 2023-08, Vol.40 (8), p.1036

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn5113874-20220812-00541 ;PMID: 37532508

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18
Prenatal diagnosis for a fetus with Walker-Warburg syndrome
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Article
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Prenatal diagnosis for a fetus with Walker-Warburg syndrome

Zhonghua yi xue yi chuan xue za zhi, 2023-05, Vol.40 (5), p.572

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20220425-00279 ;PMID: 37102292

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19
Carrier screening and prenatal diagnosis for thalassemia-associated mutations in Jiaxing area of Zhejiang
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Carrier screening and prenatal diagnosis for thalassemia-associated mutations in Jiaxing area of Zhejiang

Zhonghua yi xue yi chuan xue za zhi, 2023-03, Vol.40 (3), p.295

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20220121-00054 ;PMID: 36854404

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20
Genetic analysis of a fetus with cryptophthalmos due to variants of FREM2 gene
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Genetic analysis of a fetus with cryptophthalmos due to variants of FREM2 gene

Zhonghua yi xue yi chuan xue za zhi, 2024-05, Vol.41 (5), p.606

ISSN: 1003-9406 ;DOI: 10.3760/cma.j.cn511374-20230915-00135 ;PMID: 38684310

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