Works matching IS 00166723 AND DT 2017 AND VI 99
Results: 2
GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders.
- Published in:
- Genetics Research, 2017, v. 99, p. N.PAG, doi. 10.1017/S0016672316000148
- By:
- Publication type:
- Article
Effective experimental validation of miRNA targets using an improved linker reporter assay.
- Published in:
- Genetics Research, 2017, v. 99, p. N.PAG, doi. 10.1017/S001667231600015X
- By:
- Publication type:
- Article