The present invention provides methods of identifying mutations in nucleic acid. Also provided herein are methods of identifying subjects having Hirschsprung disease risk and diagnostic markers for Hirschsprung disease.
申请公布号
WO2006128042(A3)
申请公布日期
2007.08.09
申请号
WO2006US20580
申请日期
2006.05.26
申请人
THE JOHNS HOPKINS UNIVERSITY;CHAKRAVARTI, ARAVINDA;EMISON, EILEEN, SPROAT;MCCALLION, ANDREW, SMYTHE;GREEN, ERIC
发明人
CHAKRAVARTI, ARAVINDA;EMISON, EILEEN, SPROAT;MCCALLION, ANDREW, SMYTHE;GREEN, ERIC
