Array technology in prenatal diagnosis-Reference-Cited by-同舟云学术

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Array technology in prenatal diagnosis

Published:2011-04 Issue:2 Volume:16 Page:94-98
ISSN:1744-165X
Container-title:Seminars in Fetal and Neonatal Medicine
language:en
Short-container-title:Seminars in Fetal and Neonatal Medicine

Author:

Zuffardi Orsetta,Vetro Annalisa,Brady Paul,Vermeesch Joris

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference49 articles.

1. Chromosome analysis of human amniotic fluid cells;Steel;Lancet,1966

2. Intrauterine diagnosis and management of genetic defects;Jacobson;Am J Obstet Gynecol,1967

3. Some cytogenetic aspects of habitual abortion;Jacobson;Am J Obstet Gynecol,1967

4. Antenatal detection of hereditary disorders;Nadler;Pediatrics,1968

5. Prenatal diagnosis. Fetoscopy;Nicolaides;Br J Hosp Med,1984

Cited by 19 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. Informed Decision-Making in the Context of Prenatal Chromosomal Microarray;Journal of Genetic Counseling;2018-03-07

2. Patient preferences for prenatal testing of microdeletion and microduplication syndromes;Prenatal Diagnosis;2016-01-27

3. Whole-genome array as a first-line cytogenetic test in prenatal diagnosis;Ultrasound in Obstetrics & Gynecology;2015-04

4. Microdeletions/duplications involvingTBX1gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescencein-situhybridization;Ultrasound in Obstetrics & Gynecology;2013-12-26

5. Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection;Human Genetics;2013-09-28

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