Published in Cytogenet Cell Genet on January 01, 1995
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. Am J Hum Genet (1997) 1.99
X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27. J Med Genet (1999) 1.33
A submicroscopic deletion in Xq26 associated with familial situs ambiguus. Am J Hum Genet (1997) 0.98
Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet (1998) 0.87
Renpenning syndrome maps to Xp11. Am J Hum Genet (1998) 0.82
Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis. Am J Hum Genet (1997) 0.81
Androgen insensitivity with mental retardation: a contiguous gene syndrome? J Med Genet (1997) 0.80
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26. J Med Genet (1998) 0.77
IXDB, an X chromosome integrated database. Nucleic Acids Res (1998) 0.75
Improved genetic mapping of X linked retinoschisis. J Med Genet (1996) 0.75