References
- McKusick V A. Mendelian Inheritance in Man. Johns Hopkins University Press, Baltimore 1990
- Lameris H J. Ichthyosis follicularis. Ned Tijdschr Geneesk 1905; 41: 1524
- Siemens H W. Ueber einen, in der menschlichen Pathologie noch nicht beobachteten Vererbungsmodus: dominant geschlechts-gebundeneVererbung. Arch Rass u Ges Biol 1925; 17: 47–61
- Kuokkanen K. Keratosis follicularis spinulosa decalvans in a family from Northern Finland. Acta Dermatol Venereol 1971; 51: 146–150
- Holthuis P. Keratosis follicularis spinulosa decalvans (Siemens). Ophthalmologica 1943; 106: 325
- Waardenburg P J, Franceschetti A, Klein D. Genetics and Ophthalmology. Blackwell, Oxford 1961; 1: 517–521
- Franceschetti A, Jaccottet M, Jadassohn W. Manifestations cornéennes dans la keratosis follicularis spinulosa decalvans (Siemens). Ophthalmologica 1957; 133: 259
- Jonkers GH. Hyperkeratosis follicularis and cornea degeneration. Ophthalmologica 1951; 120: 365–367
- Kohler U, Muller W, Schubert H, Lukassek B. Beitrag zum Siemens-I-Syndrom. Klin Mbl Augenheilk 1981; 179: 123–127
- Van Osch L DM, Oranje A P, Keukens F M, Van Voorst, Vader P C, Veldman E. Keratosis follicularis spinulosa decalvans. J Med Genet 1992; in press
- Davies K E, Mandel J L, Monaco A P, Nussbaum R L, Willard H F. Report of the committee on the genetic constitution of the X-chromosome. Cytogenet Cell Genet 1990; 55: 254–313
- Lathrop G M, Lalouel J M. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984; 36: 460–465
- Sieving P A, Bingham E L, Roth MS, et al. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1–p22.3 probes. Am J Hum Genet 1990; 47: 616–621
- Bergen A AB, Platje E JM, Craig I, et al. Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis. Ophthalm Paediatr Genet 1991; 12: 99–103