Wang, I; Franco, B; Ferrero, G B et al. (1995) High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1). Genomics 26:229-38
|
van Slegtenhorst, M A; Bassi, M T; Borsani, G et al. (1994) A gene from the Xp22.3 region shares homology with voltage-gated chloride channels. Hum Mol Genet 3:547-52
|
Lindsay, E A; Grillo, A; Ferrero, G B et al. (1994) Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. Am J Med Genet 49:229-34
|
Wapenaar, M C; Bassi, M T; Schaefer, L et al. (1993) The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions. Hum Mol Genet 2:947-52
|
Rugarli, E I; Ballabio, A (1993) Kallmann syndrome. From genetics to neurobiology. JAMA 270:2713-6
|
Casey, B; Devoto, M; Jones, K L et al. (1993) Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Nat Genet 5:403-7
|
Ballabio, A; Willard, H F (1992) Mammalian X-chromosome inactivation and the XIST gene. Curr Opin Genet Dev 2:439-47
|