TY  - GEN
AU  - Fontana,L
AU  - Bedeschi,M F
AU  - Maitz,S
AU  - Cereda,A
AU  - Faré,C
AU  - Motta,S
AU  - Seresini,A
AU  - D'Ursi,P
AU  - Orro,A
AU  - Pecile,V
AU  - Calvello,M
AU  - Selicorni,A
AU  - Lalatta,F
AU  - Milani,D
AU  - Sirchia,S M
AU  - Miozzo,M
AU  - Tabano,S
TI  - Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
SN  - 1559-2308
PY  - 2019///0306
KW  - Adaptor Proteins, Signal Transducing
KW  - chemistry
KW  - Adolescent
KW  - Apoptosis Regulatory Proteins
KW  - Beckwith-Wiedemann Syndrome
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 15
KW  - DNA Methylation
KW  - Female
KW  - Genomic Imprinting
KW  - Humans
KW  - Infant
KW  - Kruppel-Like Transcription Factors
KW  - Male
KW  - Mutation, Missense
KW  - Silver-Russell Syndrome
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1080/15592294.2018.1514230
ER  -