标题
Preference for secondary findings in prenatal and pediatric exome sequencing
作者
关键词
-
出版物
PRENATAL DIAGNOSIS
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2021-05-31
DOI
10.1002/pd.5973
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
- (2020) Neeta L. Vora et al. GENETICS IN MEDICINE
- Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability
- (2020) Jennifer Malinowski et al. GENETICS IN MEDICINE
- Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis
- (2020) Teresa N. Sparks et al. NEW ENGLAND JOURNAL OF MEDICINE
- Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
- (2019) Slavé Petrovski et al. LANCET
- Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
- (2019) Jenny Lord et al. LANCET
- Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature
- (2018) Hadley Stevens Smith et al. GENETICS IN MEDICINE
- Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis
- (2018) et al. PRENATAL DIAGNOSIS
- Offering a choice between NIPT and invasive PND in prenatal genetic counseling: the impact of clinician characteristics on patients’ test uptake
- (2018) Sanne L. van der Steen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
- (2018) M. Ragan Hart et al. GENETICS IN MEDICINE
- Promises, pitfalls and practicalities of prenatal whole exome sequencing
- (2017) Sunayna Best et al. PRENATAL DIAGNOSIS
- Choices of incidental findings of individuals undergoing genome wide sequencing, a single center's experience
- (2016) C.L Bishop et al. CLINICAL GENETICS
- Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
- (2016) Sarah S. Kalia et al. GENETICS IN MEDICINE
- Experiences with obtaining informed consent for genomic sequencing
- (2015) Barbara A. Bernhardt et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Reporting genomic secondary findings: ACMG members weigh in
- (2014) Maren T. Scheuner et al. GENETICS IN MEDICINE
- Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children
- (2013) J.C. Sapp et al. CLINICAL GENETICS
- Incidental findings in clinical genomics: a clarification
- (2013) GENETICS IN MEDICINE
- Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing
- (2013) Layla Shahmirzadi et al. GENETICS IN MEDICINE
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
- (2013) Robert C. Green et al. GENETICS IN MEDICINE
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