Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant-Reference-Cited by-同舟云学术

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Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant

Published:2007 Issue:7 Volume:27 Page:616-621
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Lapaire Olav,Lu Xin-Yan,Johnson Kirby L.,Jarrah Zina,Stroh Helene,Cowan Janet M.,Tantravahi Umadevi,Bianchi Diana W.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference29 articles.

1. Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization

2. Detection of low-level mosaicism by array CGH in routine diagnostic specimens

3. Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to growin vitro

4. Noninvasive Prenatal Diagnosis of Fetal Rhesus D

5. Large Amounts of Cell-free Fetal DNA Are Present in Amniotic Fluid

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Multilevel regression modeling for aneuploidy classification and physical separation of maternal cell contamination facilitates the QF-PCR based analysis of common fetal aneuploidies;PLOS ONE;2019-08-20

2. Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation;Efficacy and Mechanism Evaluation;2017-02

3. Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid;Prenatal Diagnosis;2016-05-17

4. Cell-free fetal DNA in amniotic fluid supernatant for prenatal diagnosis;Cellular and Molecular Biology;2016-04-30

5. Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues;The Application of Clinical Genetics;2016-02

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