Congenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders.
Eggermann, Thomas
Congenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders. [electronic resource] - The Journal of pediatrics Oct 2013 - 1202-7 p. digital
Publication Type: Clinical Conference; Journal Article
1097-6833
10.1016/j.jpeds.2013.05.017 doi
Abnormalities, Multiple--genetics
Adolescent
Child
Child, Preschool
Chromosome Mapping
DNA Methylation
Epigenesis, Genetic
Female
Genetic Association Studies
Genomic Imprinting
Heterozygote
Humans
Infant
Male
Phenotype
Syndrome
Uniparental Disomy--genetics
Congenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders. [electronic resource] - The Journal of pediatrics Oct 2013 - 1202-7 p. digital
Publication Type: Clinical Conference; Journal Article
1097-6833
10.1016/j.jpeds.2013.05.017 doi
Abnormalities, Multiple--genetics
Adolescent
Child
Child, Preschool
Chromosome Mapping
DNA Methylation
Epigenesis, Genetic
Female
Genetic Association Studies
Genomic Imprinting
Heterozygote
Humans
Infant
Male
Phenotype
Syndrome
Uniparental Disomy--genetics