Variants of uncertain significance in prenatal microarrays: a retrospective cohort study-Reference-Cited by-同舟云学术

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Variants of uncertain significance in prenatal microarrays: a retrospective cohort study

Published:2020-08-18 Issue:2 Volume:128 Page:431-438
ISSN:1470-0328
Container-title:BJOG: An International Journal of Obstetrics & Gynaecology
language:en
Short-container-title:BJOG: Int J Obstet Gy

Author:

Mardy AH¹^ORCID,Wiita AP²,Wayman BV³,Drexler K⁴,Sparks TN¹^ORCID,Norton ME¹

Affiliation:

1. Division of Maternal Fetal Medicine University of California San Francisco CA USA

2. Department of Laboratory Medicine University of California San Francisco CA USA

3. Cytogenetics Laboratory University of California San Francisco CA USA

4. Prenatal Diagnostic Center University of California San Francisco CA USA

Publisher

Wiley

Subject

Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1471-0528.16427

Reference19 articles.

1. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

2. Committee Opinion No. 682: Microarrays and next‐generation sequencing technology: the use of advanced genetic diagnostic tools in obstetrics and gynecology. Obs Gynecol2016;128(6).e262–e268.

3. Women’s experiences receiving abnormal prenatal chromosomal microarray testing results

4. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

5. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases

Cited by 12 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. Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: a retrospective population-based cohort study;BMC Pediatrics;2024-08-22

2. From uncertain to certain—how to proceed with variants of uncertain significance;Middle East Fertility Society Journal;2024-08-16

3. Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: A retrospective population-based cohort study;2024-04-19

4. Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array;Journal of Personalized Medicine;2024-03-08

5. Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations;Genes;2023-09-26

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