Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules

Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maint...

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Veröffentlicht in:Journal of the American Academy of Child and Adolescent Psychiatry 2000-03, Vol.39 (3), p.386-389
Hauptverfasser: EVERMAN, DAVID B., CASSIDY, SUZANNE B.
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container_title Journal of the American Academy of Child and Adolescent Psychiatry
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creator EVERMAN, DAVID B.
CASSIDY, SUZANNE B.
description Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maintaining this phenomenon. They also discuss the molecular bases for two disorders in which imprinting is involved--Prader-Willi and Angelman syndromes.
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source MEDLINE; Applied Social Sciences Index & Abstracts (ASSIA); Journals@Ovid Ovid Autoload; Access via ScienceDirect (Elsevier)
subjects Angelman Syndrome - genetics
Biological and medical sciences
Child
Child development
Child, Preschool
Children & youth
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 15
Complex syndromes
Female
Genetics
Genomic Imprinting - genetics
Humans
Ligases - genetics
Male
Medical disorders
Medical genetics
Medical sciences
Neurology
Prader-Willi Syndrome - diagnosis
Prader-Willi Syndrome - genetics
Ubiquitin-Protein Ligases
title Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules
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