Cytogenetic analysis of 6,142 amniocentesis cases: A 6-year single centre experience
Author:
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology
Link
http://www.tandfonline.com/doi/pdf/10.3109/01443615.2014.919577
Reference29 articles.
1. ACOG Practice Bulletin No. 77: Screening for Fetal Chromosomal Abnormalities
2. Changes in the Utilization of Prenatal Diagnosis
3. Challenging the Strategy of Maternal Age–Based Prenatal Genetic Counseling
4. Advanced maternal age as a sole indication for genetic amniocentesis; risk-benefit analysis based on a large database reflecting the current common practice
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2. Clinical Significance of Conventional Karyotype and QF-PCR in Detection of Fetal Chromosomal Abnormalities;Journal of Fetal Medicine;2016-11-25
3. Impact of fetal or child loss on parents’ perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions;Midwifery;2016-03
4. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect;Molecular Cytogenetics;2015-12
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