Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and SIM1[original query] |
---|
Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients. Molecular genetics and metabolism 2016 Jan . Geets Ellen, Zegers Doreen, Beckers Sigri, Verrijken An, Massa Guy, Van Hoorenbeeck Kim, Verhulst Stijn, Van Gaal Luc, Van Hul W |
DNA sequencing and copy number variation analysis of MCHR2 in a cohort of Prader Willi like (PWL) patients. Obesity research & clinical practice 2017 Oct . Geets Ellen, Aerts Evi, Verrijken An, Van Hoorenbeeck Kim, Verhulst Stijn, Van Gaal Luc, Van Hul W |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: