| 1 | HTC2 |
| X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3. | |
| Zhu H, Shang D, Sun M, Choi S, Liu Q, Hao J, Figuera LE, Zhang F, Choy KW, Ao Y, Liu Y, Zhang XL, Yue F, Wang MR, Jin L, Patel PI, Jing T, Zhang X. | |
| Am J Hum Genet 88(6):819-26. 2011 | |
| 2 | HTC2 |
| Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait. | |
| Tadin-Strapps M, Salas-Alanis JC, Moreno L, Warburton D, Martinez-Mir A, Christiano AM. | |
| Clin Genet 63(5):418-22. 2003 | |
| 3 | HTC2 |
| Mapping of the congenital generalized hypertrichosis locus to chromosomeXq24-q27.1. | |
| Figuera LE, et al. | |
| Nat Genet 10 : 202-207. 1995 | |