| 1 | AGOTC, PRRX1 |
| PRRX1 is mutated in a fetus with agnathia-otocephaly. | |
| Sergi C, Kamnasaran D. | |
| Clin Genet 79(3):293-5. doi: 10.1111/j.1399-0004.2010.01531.x. No abstract available. 2011 | |
| 2 | AGOTC |
| Auriculo-condylar syndrome: additional patients. | |
| Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Kokitsu-Nakata NM. | |
| Am J Med Genet 112(2):209-14. 2002 | |
| 3 | AGOTC |
| Transmission of the dysgnathia complex from mother to daughter. | |
| Erlich MS, Cunningham ML, Hudgins L. | |
| Am J Med Genet 95(3):269-74. 2000 | |
| 4 | AGOTC |
| Familial agnathia-holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance. | |
| Krassikoff N, Sekhon GS. | |
| Am J Med Genet 34(2):255-7. No abstract available. 1989 | |