Gene: [0Xq273/FMR1] fragile X mental retardation 1 (Martin-Bell syndrome); fragile site Xq27.3, folic acid type, rare; Martin-Bell syndrome (mental retardation/macroorchidism); [FRAXA MRXFRA ]
REL |
GEM:0Xq28/FMR2. |
LIK |
GEM:00.0/FMR1L2. |
REF |
MAP,POL "Arveiller &: AJHG, 42, 380-389, 1988 MUT "Mila M &: Hum Genet, 100, N5-6, 503-507, 1997 PND "Sutherland &: New Engl J Med, 325, N24, 1720-1722, 1991 MAP "Warren ST &: Science, 237, 420-423, 1987 |
KEY |
neu, devd, chr, tri |
CLA |
coding, basic |
LOC |
0X q27.3 |
MIM |
MIM: 309550 |
SYN |
FRAXA MRXFRA |