Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma.

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Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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name

Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

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Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

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label

Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

@en

Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

@nl

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Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

@en

Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma.

@nl

P1476

Haplotype-based Noninvasive Pr ...... Sequencing of Maternal Plasma

@en

P2093

Asan

http://www.w3.org/2001/XMLSchema#string

Chao Chen

http://www.w3.org/2001/XMLSchema#string

Huiwen Zhang

http://www.w3.org/2001/XMLSchema#string

Jun Ye

http://www.w3.org/2001/XMLSchema#string

Lianshu Han

http://www.w3.org/2001/XMLSchema#string

Wenjuan Qiu

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Xuefan Gu

http://www.w3.org/2001/XMLSchema#string

Yuan Yuan

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P2860

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

A tutorial on hidden Markov models and selected applications in speech recognition

Family conditions and dietary control in phenylketonuria.

Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma.

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.

A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection.

Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.

Neonatal screening for congenital hypothyroidism and phenylketonuria in China.

P304

161

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scholarly article

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10.1038/S41598-017-18358-Y

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English

P433

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P478

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Yaoshen Wang

P577

2018-01-09T00:00:00Z

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29317692

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5760544

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