Temple syndrome as a result of isolated hypomethylation of the 14q32 imprinted DLK1/MEG3 region.

Briggs, Tracy A

Temple syndrome as a result of isolated hypomethylation of the 14q32 imprinted DLK1/MEG3 region. [electronic resource] - American journal of medical genetics. Part A Jan 2016 - 170-5 p. digital

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

1552-4833

10.1002/ajmg.a.37400 doi


Abnormalities, Multiple--genetics
Adolescent
Calcium-Binding Proteins
Chromosomes, Human, Pair 14--genetics
DNA Methylation--genetics
Developmental Disabilities--genetics
Female
Genomic Imprinting--genetics
Humans
Intercellular Signaling Peptides and Proteins--genetics
Membrane Proteins--genetics
Phenotype
RNA, Long Noncoding--genetics
Uniparental Disomy--genetics