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Results of search for 'au:"Wang, Benjing"'
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Authors
Chen, Yaping
Chen, Ying
Cram, David S
Dai, Jianrong
Gao, Ang
Jiang, Dong
Li, Haibo
Li, Hong
Li, Qiong
Liu, Minjuan
Liu, Shuang
Ma, Jun
Mao, Jun
Wang, Benjing
Wang, Leilei
Wang, Qi
Wang, Ting
Yang, Yuqi
Yu, Bin
Zhang, Qin
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Topics
17-alpha-Hydroxyprogesterone
Adolescent
Adrenal Hyperplasia, Congenital
Child
Child, Preschool
Connexin 26
Connexins
Female
Genotype
Humans
Infant
Infant, Newborn
Male
Membrane Transport Proteins
Mutation
Neonatal Screening
Sulfate Transporters
blood
genetics
methods
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Chinese
English
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Your search returned 9 results.
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Results
1.
[Multicenter investigation on the impact of newborn infants' gestational age and birth weight on the level of 17α-hydroxyprogesterone].
[electronic resource]
by
Zhang, Qin
Wang, Benjing
Chen, Yaping
Jiang, Dong
Chen, Ying
Producer:
20150423
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 52
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No items available.
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2.
Application of Next-Generation Sequencing Following Tandem Mass Spectrometry to Expand Newborn Screening for Inborn Errors of Metabolism: A Multicenter Study.
[electronic resource]
by
Yang, Yuqi
Wang, Leilei
Wang, Benjing
Liu, Shuang
Yu, Bin
Wang, Ting
Publication details:
Frontiers in genetics
2019
In:
Frontiers in genetics
vol. 10
Online resources:
Available from publisher's website
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No items available.
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3.
Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.
[electronic resource]
by
Wang, Benjing
Liu, Minjuan
Yan, Wenhua
Mao, Jun
Jiang, Dong
Li, Hong
Chen, Ying
Producer:
20140701
In:
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
vol. 26
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4.
New Ratios for Performance Improvement for Identifying Acyl-CoA Dehydrogenase Deficiencies in Expanded Newborn Screening: A Retrospective Study.
[electronic resource]
by
Wang, Benjing
Zhang, Qin
Gao, Ang
Wang, Qi
Ma, Jun
Li, Hong
Wang, Ting
Publication details:
Frontiers in genetics
2019
In:
Frontiers in genetics
vol. 10
Online resources:
Available from publisher's website
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5.
3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary?
[electronic resource]
by
Wang, Huaiyan
Liu, Shuang
Wang, Benjing
Yang, Yuqi
Yu, Bin
Wang, Leilei
Wang, Ting
Producer:
20200511
In:
Journal of pediatric endocrinology & metabolism : JPEM
vol. 32
Online resources:
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6.
SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.
[electronic resource]
by
Li, Haibo
Wang, Benjing
Liu, Deyuan
Wang, Ting
Li, Qiong
Wang, Wei
Li, Hong
Producer:
20160101
In:
Genomics
vol. 106
Online resources:
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7.
Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population.
[electronic resource]
by
Wang, Ting
Ma, Jun
Zhang, Qin
Gao, Ang
Wang, Qi
Li, Hong
Xiang, Jingjing
Wang, Benjing
Publication details:
Frontiers in genetics
2019
In:
Frontiers in genetics
vol. 10
Online resources:
Available from publisher's website
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8.
Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.
[electronic resource]
by
Zhu, Qin
Chen, Ying
Dai, Jianrong
Wang, Benjing
Liu, Minjuan
Wang, Yun
Tao, Jianying
Li, Hong
Producer:
20160202
In:
Translational pediatrics
vol. 4
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9.
Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.
[electronic resource]
by
Chen, Ying
Liu, Yiqian
Wang, Benjing
Mao, Jun
Wang, Ting
Ye, Kan
Ye, Yanlin
Cram, David S
Li, Hong
Producer:
20170726
In:
Prenatal diagnosis
vol. 36
Online resources:
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