Literature DB >> 24925152

Genetics of common malformations.

John M Graham1, Raoul C Hennekam2.   

Abstract

Advanced technology has recently allowed us to study rare Mendelian disorders in an unprecedented manner. The same technology should allow us also to study more common malformations. Many of these are not caused by a variant in a single Mendelian gene but by interplay between series of genetic variants and exogenous influences. Likely the site from which the DNA is derived is of great importance in studying malformations as mosaicism may be much more common than earlier anticipated. Factors other than simple variants in our genomic DNA should be considered in the studies as well. Not only is recognition of someone's liability to disease important, but also determining exogenous factors involved in malformations should receive more attention as it may allow us decrease the burden of malformations in humans.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Epidemiology; Epigenetics; Genetics; Malformations; Mosaicism; Prevention; Teratogenics

Mesh:

Year:  2014        PMID: 24925152     DOI: 10.1016/j.ejmg.2014.05.007

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  2 in total

1.  An integrated approach for analyzing clinical genomic variant data from next-generation sequencing.

Authors:  Erin L Crowgey; Deborah L Stabley; Chuming Chen; Hongzhan Huang; Katherine M Robbins; Shawn W Polson; Katia Sol-Church; Cathy H Wu
Journal:  J Biomol Tech       Date:  2015-04

2.  The Financial Impact of Genetic Diseases in a Pediatric Accountable Care Organization.

Authors:  Katherine E Miller; Richard Hoyt; Steve Rust; Rachel Doerschuk; Yungui Huang; Simon M Lin
Journal:  Front Public Health       Date:  2020-02-28
  2 in total

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