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Archives of Disease in Childhood - Fetal and Neonatal Edition 2007;92:F308-F314; doi:10.1136/adc.2004.062968
Copyright © 2007 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.

REVIEW

Genetic aspects of birth defects: new understandings of old problems

Katrina R Prescott1 and Andrew O M Wilkie2

1 Department of Clinical Genetics, Churchill Hospital, Oxford, UK
2 Weatherall Institute of Molecular Medicine, University of Oxford, UK

Correspondence to:
Correspondence to:
Andrew O M Wilkie
Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DS, UK; awilkie{at}hammer.imm.ox.ac.uk

ABSTRACT

Over the past two decades, combined advances in genetics, developmental biology and biochemistry have transformed the study of human birth defects. This review describes the importance of genome architecture, parent of origin effects (imprinting), molecular pathophysiology, developmental pathways, mosaicism and cancer predisposition syndromes in the understanding of birth defects. This knowledge can be applied to improve diagnostic accuracy, prognostic information, counselling and sometimes even treatment of these conditions.

Abbreviations: CGH, comparative genomic hybridisation; FISH, fluorescence in-situ hybridisation; FGFR, fibroblast growth factor receptor; MCA/MR, multiple congenital abnormality/mental retardation; UPD, uniparental disomy

Keywords: genetics; imprinting; microarray; microdeletion; mosaicism


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