Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation. [electronic resource]
- American journal of medical genetics. Part A Feb 2012
- 423-8 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1552-4833
10.1002/ajmg.a.34412 doi
Calcium-Binding Proteins Child, Preschool Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 7 DNA Methylation--genetics Humans Intercellular Signaling Peptides and Proteins--genetics Male Membrane Proteins--genetics Proteins--genetics RNA, Long Noncoding Silver-Russell Syndrome--diagnosis Uniparental Disomy--diagnosis