Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies-Reference-Cited by-同舟云学术

Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies

Published:2015-08-03 Issue:11 Volume:35 Page:1073-1078
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Alamillo Christina L.¹,Powis Zöe¹,Farwell Kelly¹,Shahmirzadi Layla¹,Weltmer Elaine C.¹,Turocy John²,Lowe Thomas³,Kobelka Christine⁴,Chen Emily⁴,Basel Donald⁵,Ashkinadze Elena⁶,D'Augelli Lisa⁷,Chao Elizabeth¹⁸,Tang Sha¹

Affiliation:

1. Ambry Genetics; Aliso Viejo CA USA

2. Genetics Department; Kaiser Permanente; Clovis CA USA

3. Thomas Lowe, MD; Private Practice; Boca Raton FL USA

4. Genetics Department; Kaiser Permanente; San Francisco CA USA

5. Division of Genetics; Medical College of Wisconsin; Milwaukee WI USA

6. Division of Maternal-Fetal Medicine; Rutgers Robert Wood Johnson Medical School; New Brunswick NJ USA

7. Integrated Genetics; Westborough MA USA

8. Department of Pediatrics; University of California Irvine; Irvine CA USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4648/fullpdf

Reference33 articles.

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4. The usefulness of whole-exome sequencing in routine clinical practice;Iglesias;Genet Med,2014

5. Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders;Soden;Sci Transl Med,2014

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