Prenatal and preimplantation genetic diagnosis for single gene disorders: A population-based study from 1977 to 2016

Author:

Poulton Alice1ORCID,Lewis Sharon12,Hui Lisa134ORCID,Halliday Jane L.12

Affiliation:

1. Public Health Genetics; Murdoch Children's Research Institute, Royal Children's Hospital; Parkville Victoria Australia

2. Department of Paediatrics; University of Melbourne; Parkville Victoria Australia

3. Department of Perinatal Medicine; Mercy Hospital for Women; Heidelberg Victoria Australia

4. Department of Obstetrics and Gynaecology; University of Melbourne; Parkville Victoria Australia

Funder

National Health and Medical Research Council Senior Research Fellowship

National Health and Medical Research Council Early Career Fellowship

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference35 articles.

1. The human gene mutation database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies;Stenson;Hum Genet,2017

2. Mendelian genetics: patterns of inheritance and single-gene disorders;Chial;Nat Educ,2005

3. Prenatal diagnosis of single gene disorders;Eason;Obstet Gynaecol Reprod Med,2010

4. Advances in the prenatal diagnosis of monogenic disorders;Chitty;Prenat Diagn,2018

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