| scholarly article | Q13442814 |
| P50 | author | XiaoFang Sun | Q88161470 |
| P2093 | author name string | Yang Wang | |
| Min Chen | |||
| Chunsheng Zhang | |||
| Haoxian Li | |||
| Fuman Jiang | |||
| Yuhuan Xie | |||
| Weiqiang Liu | |||
| Xiaojing Zeng | |||
| Yexing Xian | |||
| Shuming Ouyang | |||
| Bole Du | |||
| Yulai Guo | |||
| P2860 | cites work | Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: a feasibility study | Q78014625 |
| Chorionic villus sampling for early prenatal diagnosis: Experience at a mainland Chinese hospital | Q88044459 | ||
| Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration | Q28264933 | ||
| Beta-thalassemia | Q28272228 | ||
| Analysis of Cell-Free DNA in Maternal Blood in Screening For Aneuploidies: Updated Meta-Analysis. | Q30234867 | ||
| Updates of the HbVar database of human hemoglobin variants and thalassemia mutations | Q30486431 | ||
| Getting more from digital SNP data | Q31028867 | ||
| Shape-IT: new rapid and accurate algorithm for haplotype inference | Q33393477 | ||
| The prevalence of thalassemia in mainland China: evidence from epidemiological surveys | Q33680932 | ||
| Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma | Q33682367 | ||
| New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma. | Q33755108 | ||
| Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China. | Q33855578 | ||
| High prevalence of thalassemia in migrant populations in Guangdong Province, China | Q34169004 | ||
| A general approach for haplotype phasing across the full spectrum of relatedness | Q34415720 | ||
| The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China | Q35108208 | ||
| Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis | Q35209735 | ||
| Haplotype phasing: existing methods and new developments | Q35554981 | ||
| Improvement in strategies for the non-invasive prenatal diagnosis of Huntington disease | Q36970248 | ||
| Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
| Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage | Q37745036 | ||
| Non-invasive prenatal diagnosis: progress and potential | Q38208530 | ||
| Noninvasive fetal genomic, methylomic, and transcriptomic analyses using maternal plasma and clinical implications | Q38331302 | ||
| Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA | Q38549770 | ||
| Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis. | Q38770436 | ||
| Noninvasive Prenatal DNA Testing: The Vanguard of Genomic Medicine | Q38812354 | ||
| Thalassaemia | Q39708856 | ||
| Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia | Q40028010 | ||
| Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia. | Q40057027 | ||
| New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma. | Q40078199 | ||
| Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma. | Q41475376 | ||
| Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma | Q47391690 | ||
| Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping | Q47900162 | ||
| Non-invasive prenatal diagnosis of beta-thalassemia by semiconductor sequencing: a feasibility study in the sardinian population. | Q48150902 | ||
| Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing. | Q54184929 | ||
| Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus | Q56937251 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma | Q73406198 | ||
| P433 | issue | 11 | |
| P304 | page(s) | e963 | |
| P577 | publication date | 2019-09-30 | |
| P1433 | published in | Molecular genetics & genomic medicine | Q27724709 |
| P1476 | title | Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband | |
| P478 | volume | 7 |
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