Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies-Reference-Cited by-同舟云学术

Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies

Published:2022-02 Issue:7 Volume:42 Page:822-830
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Wang Yiming¹²,Greenfeld Elena³⁴,Watkins Nicholas⁴,Belesiotis Peter⁵,Zaidi Syed H.⁵,Marshall Christian³⁵,Thiruvahindrapuram Bhooma⁶,Shannon Patrick³⁴,Roifman Maian¹⁷,Chong Karen⁷^ORCID,Chitayat David¹⁷,Stavropoulos Dimitri James³⁵,Noor Abdul³⁴^ORCID

Affiliation:

1. Division of Clinical and Metabolic Genetics, Department of Pediatrics The Hospital for Sick Children University of Toronto Toronto Ontario Canada

2. Medical Genetics and Genomics Residency Program University of Toronto Toronto Ontario Canada

3. Department of Laboratory Medicine and Pathobiology University of Toronto Toronto Ontario Canada

4. Division of Diagnostic Medical Genetics, Department of Pathology and Laboratory Medicine Mount Sinai Hospital Toronto Ontario Canada

5. Division of Genome Diagnostics, Department of Paediatric Laboratory Medicine The Hospital for Sick Children Toronto Ontario Canada

6. The Centre for Applied Genomics The Hospital for Sick Children Toronto Ontario Canada

7. The Prenatal Diagnosis and Medical Genetics Program Department of Obstetrics and Gynecology Mount Sinai Hospital Toronto Ontario Canada

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6108

Reference25 articles.

1. Risk of major congenital malformations in relation to maternal overweight and obesity severity: cohort study of 1.2 million singletons

2. Prenatal and pre-implantation genetic diagnosis

3. Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada

4. Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories

5. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

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