Table 1.
Patient ID | TCF2 | LHX1 |
RK104 | ||
RK105 | 1654-21 C/T | |
RK106 | 841+26 A/G | |
RK107 | 841+26 A/G | |
RK111 | 1654-21 C/T | NO DNA |
RK112 | 1653+48insC; 1654-21 C/T | |
RK113 | 1654-21 T/T | |
RK114 | 1654-21 C/T | |
RK115 | 170+42 G/T | |
RK116 | 1654-21 C/T | |
RK117 | ||
RK118 | 676-34 C/T; 841+26 A/G | |
RK119 | 841+26 A/G | |
RK120 | 1654-21 C/T | |
RK121 | 1653+48insC | |
RK122 | 1654-21 T/T | |
RK123 | 1654-21 C/T | |
RK124 | ||
RK125 | 1653+48insC | |
RK126 |
List of the known polymorphisms disclosed by the mutational analysis of LHX1 and TCF2 genes in 20 selected chromosomally normal MRKH females, tested negative for 17q12 deletion.