The prevalence of prenatal sonographic findings in postnatal diagnostic exome sequencing performed for neurocognitive phenotypes: A cohort study-Reference-Cited by-同舟云学术

The prevalence of prenatal sonographic findings in postnatal diagnostic exome sequencing performed for neurocognitive phenotypes: A cohort study

Published:2022-01-24 Issue:6 Volume:42 Page:717-724
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Sukenik‐Halevy Rivka¹²^ORCID,Perlman Sharon²³,Ruhrman‐Shahar Noa¹,Engel Offra⁴,Orenstein Naama⁵,Gonzaga‐Jauregui Claudia⁶,Shuldiner Alan R.⁶,Magal Nurit¹,Hagari Ofir¹,Azulay Noy¹,Lidzbarsky Gabriel Arie¹,Bazak Lily¹,Basel‐Salmon Lina¹²⁵⁷,

Affiliation:

1. Raphael Recanati Genetic Institute Rabin Medical Center – Beilinson Hospital Petah Tikva Israel

2. Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

3. Ultrasound Unit Helen Schneider Women's Hospital Rabin Medical Center Petah Tikva Israel

4. Department of Obstetrics and Gynecology Meir Medical Center Kfar Saba Israel

5. Pediatric Genetics Clinic, Schneider Children's Medical Center of Israel Petah Tikva Israel

6. Regeneron Genetics Center Tarrytown New York USA

7. Felsenstein Medical Research Center Petah Tikva Israel

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6095

Reference27 articles.

1. 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

2. The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG);Monaghan KG;Genet Med Off J Am Coll Med Genet,2020

3. Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders

4. Clinical application of whole-exome sequencing across clinical indications

5. Meta‐analysis and multidisciplinary consensus statement: exome sequencing is a first‐tier clinical diagnostic test for individuals with neurodevelopmental disorders;Srivastava S;Genet Med Off J Am Coll Med Genet,2019

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