Concepedia

A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3

Annick Cabot, Jean‐Michel Rozet, S. Gerber, Isabelle Perrault, Dominique Ducroq, Asma Smahi, Eric H. Souied, Arnold Munnich, Josseline Kaplan

The American Journal of Human Genetics · 1999 · 95 citations · 22 references

DOIFull text

Open access

Concepts

References

22

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Colette Dib, Sabine Fauré, Cécile Fizames et al. · Nature · 1996 · 3K citations

, , +12

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

R.Cutler Allen, Huda Y. Zoghbi, A. Moseley et al. · PubMed · 1992 · 1.7K citations

, , +14

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · PubMed · 1985 · 1.2K citations

, , +11

X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene

Monique Jouet, André Rosenthal, Giles Armstrong et al. · Nature Genetics · 1994 · 420 citations

, , +8

Foveation dynamics in congenital nystagmus I: Fixation

Louis F. Dell’Osso, J. van der Steen, R M Steinman et al. · Documenta Ophthalmologica · 1992 · 113 citations

, , +5