Should we ‘open the kimono’ to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?

Author:

Bianchi Diana W.1ORCID

Affiliation:

1. Mother Infant Research Institute, Tufts Medical Center and Division of Genetics, Department of Pediatrics; Floating Hospital for Children; Boston MA USA

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference19 articles.

1. Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases;Pescia;Genet Med,2016

2. Whole genome evaluation of all 24 chromosomes explains unusual NIPT results and suggests additional risks;Halks-Miller;Prenat Diagn,2016

3. De Vriendt K. Clinical results of NIPT: possibilities and limitations

4. Clinical implementation of NIPT-technical and biological challenges;Brady;Clin Genet,2016

5. Increased risk for pregnancy loss, true fetal mosaicism and uniparental disomy associated with rare autosomal aneuploidies identified during non-invasive prenatal testing;Pertile;Prenat Diagn,2016

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