Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.

Fontana, L

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. [electronic resource] - Epigenetics 2018 - 897-909 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1559-2308

10.1080/15592294.2018.1514230 doi


Adaptor Proteins, Signal Transducing--chemistry
Adolescent
Apoptosis Regulatory Proteins
Beckwith-Wiedemann Syndrome--genetics
Child
Child, Preschool
Chromosomes, Human, Pair 15--genetics
DNA Methylation
Female
Genomic Imprinting
Humans
Infant
Kruppel-Like Transcription Factors--chemistry
Male
Mutation, Missense
Silver-Russell Syndrome--genetics
Young Adult