The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers-Reference-Cited by-同舟云学术

The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers

Published:2019-02-28 Issue:5 Volume:39 Page:351-360
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Durham Leslie¹²^ORCID,Papanna Ramesha³,Stevens Blair¹³,Noblin Sarah¹³,Rodriguez‐Buritica David³,Hashmi S. Shahrukh³,Krstic Nevena¹³⁴

Affiliation:

1. The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical SciencesUniversity of Texas Houston Texas

2. Department of Pediatric Development and RehabilitationRandall Children's Hospital at Legacy Emanuel Portland Oregon

3. Department of Obstetrics, Gynecology, and Reproductive SciencesMcGovern Medical School at the University of Texas Health Science Center at Houston Houston Texas

4. Department of Obstetrics and Gynecology, Morsani College of MedicineUniversity of South Florida Tampa FL

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5435

Reference24 articles.

1. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

2. Committee Opinion No. 581

3. Practice Bulletin No. 162:Prenatal diagnostic testing for genetic disorders. Obstet gynecol.2016.

4. Shield ABCaB.Chromosomal microarray analysis (CMA) for developmental delay autism spectrum disorder intellectual disability (intellectual developmental disorder) and congenital anomalies. Published2015. Accessed.

5. Aetna.Comparative genomic hybridization (CGH) policy number 0787.http://www.aetna.com/cpb/medical/data/700_799/0787.html. Published2009. Updated 11/03/2016. Accessed.

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3. Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis;Prenatal Diagnosis;2022-02-08

4. Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis;Frontiers in Genetics;2022-01-14

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