1 | XG
|
| Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp.
|
| Ellis NA, et al.
|
| Nat Genet 6 : 394-400. 1994
|
2 | XG
|
| PBDX is the XG blood group gene.
|
| Ellis NA, et al.
|
| Nat Genet 8 : 285-290. 1994
|
3 | PBDY, XG
|
| PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on Xp, and PBDY, a Y-specific duplication of PBDX, on Yq. (abstr)
|
| Ellis NA, et al.
|
| Cytogenet Cell Genet 67 : 390. 1994
|
4 | XG
|
| Identification of a new gene on Xp.
|
| Ye TZ, et al.
|
| Am J Hum Genet 51 : A138. 1992
|
5 | XG, XGR, XGRY
|
| Recombination between the X and Y chromosomes : implications for the relationship between MIC2, XG and YG.
|
| Goodfellow PJ, et al.
|
| Ann Hum Genet 51 : 161-167. 1987
|
6 | SSDI, DXS237, STS, XG
|
| Multipoint linkage analysis of steroid sulfatase (X linked ichthyosis) and distal Xp markers.
|
| Yates JRW, et al.
|
| Genomics 1 : 52-59. 1987
|
7 | CD99, STS, XG
|
| Fine mapping of the distal short arm of the human X chromosome using X/Y translocations.
|
| Geller RL, et al.
|
| Am J Hum Genet 38 : 884-890. 1986
|
8 | STS, DELXPM, KAL1, SSDI, XG
|
| X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia) : linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.
|
| Ballabio A, et al.
|
| Hum Genet 72 : 237-240. 1986
|
9 | XG
|
| A familial t(X;Y) translocation which assigns the Xg blood group locus to the region Xp22.3->pter.
|
| Ferguson-Smith MA, et al.
|
| Cytogenet Cell Genet 32 : 273-274. 1982
|
10 | XG
|
| A human quantitative polymorphism related to Xg blood groups.
|
| Goodfellow PN, et al.
|
| Nature 289 : 404-405. 1981
|