cfDNA screening and diagnosis of monogenic disorders - where are we heading? - Wikidata - awgldk - TriplyDB

cfDNA screening and diagnosis of monogenic disorders - where are we heading?

cfDNA screening and diagnosis of monogenic disorders - where are we heading?

http://www.wikidata.org/entity/Q47191639

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Large extracellular vesicles carry most of the tumour DNA circulating in prostate cancer patient plasma

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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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

@zh-my

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

cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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Prenatal Diagnosis

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cfDNA screening and diagnosis of monogenic disorders - where are we heading?

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Rossa Wai Kwun Chiu

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Beta-thalassemia

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

Haplotyping germline and cancer genomes with high-throughput linked-read sequencing

Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.

Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis.

Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage.

Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma.

Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.

Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends.

Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage.

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52-58

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scholarly article

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10.1002/PD.5207

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1

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38

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Eunice Ka Long Chiu

Winnie Wai In Hui

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2018-01-24T00:00:00Z

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29314147

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5839244

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