Begemann, Matthias

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