Patient preferences for prenatal testing of microdeletion and microduplication syndromes-Reference-Cited by-同舟云学术

Patient preferences for prenatal testing of microdeletion and microduplication syndromes

Author:

Calonico Elise¹,Blumenfeld Yair J.²³,Hudgins Louanne³⁴,Taylor Joanne³⁴

Affiliation:

1. Department of Genetics; Stanford University School of Medicine; Stanford CA USA

2. Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine; Stanford University School of Medicine; Stanford CA USA

3. Lucile Packard Children's Hospital Stanford; Palo Alto CA USA

4. Department of Pediatrics, Division of Medical Genetics; Stanford University School of Medicine; Stanford CA USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

Reference32 articles.

1. The impact of new genomic technologies in reproductive medicine;Wapner;Discov Med,2014

3. Committee Opinion No. 581: The use of chromosomal microarray analysis in prenatal diagnosis;American College of Obstetricians and Gynecologists Committee on Genetics;Obstet Gynecol,2013

4. Hall , M Panorama non-invasive prenatal screening for microdeletion syndromes 2014

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