Improved genetic mapping of X linked retinoschisis

Journal of Medical Genetics

Volumn 33, Issue 11, 1996, Pages 919-922

  George, N D L ^a,c   Payne, S J ^a   Bill, R M ^a   Barton, D E ^a   Moore, A T ^a,b   Yates, J R W ^a  

^a CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Microsatellites; Retinoschisis; X chromosome

Indexed keywords

ARTICLE; CHROMOSOME XP; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINOSCHISIS; X CHROMOSOME LINKAGE;

EID: 0029805235     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.11.919     Document Type: Article

References (16)

1. McKusick VA. Mendelian inheritance in man. 9th ed. Baltimore: Johns Hopkins University Press, 1990.
2. Deutman AF. Sex-linked juvenile retinoschisis. In: Deutman AF, ed. The hereditary dystrophies of the posterior pole of the eye. Assen, The Netherlands: Van Gorcum, 1971: 48-98.
3. Kellner U, Brummer S, Foerster MH, Wessing A. X-linked congenital retinoschisis. Graefe's Arch Clin Exp Ophthalmol 1990;228:432-7.
4. Schepens CL. Congenital retinoschisis. Klin Oczna 1988; 90:127-32.
5. George NDL, Yates JRW, Moore AT. X-linked retinoschisis. Br J Ophthalmol 1995;79:697-702.
6. Manschet WA. Pathology of hereditary juvenile retinoschisis. Arch Ophthalmol 1972;88:131-7.
7. Peachey NS, Fishman GA, Derlacki DJ, Brigell MG. Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis. Arch Ophthalmol 1987;105:513-16.
8. Forsius H, Krause U, Helve J, et al. Visual acuity in 183 cases of X-chromosomal retinoschisis. Can J Ophthalmol 1973;8:385-93.
9. Arden GB, Gorin MB, Polkinghorne PJ, Jay M, Bird AC. Detection of the carrier state of X-linked retinoschisis. Am J Ophthalmol 1988;105:590-5.
10. Boman H, Heilig P, Kolder HE, Giblett ER, Fialkow PJ. Hereditary retinoschisis: linkage studies in a family and considerations in genetic counselling. Can J Ophthalmol 1976;11:11-15.
11. Vainio-Mattila B, Eriksson AW, Forsius H. X-chromosomal recessive retinoschisis in the region of Pori. Acta Ophthalmol 1969;47:1135-48.
12. Wieacker P, Wienkert TF, Dallapicolla B, Bender K, Davies KE, Ropers HH. Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Hum Genet 1983; 64:143-5.
13. Alitalo T, Forsius H, Karna J, et al. Linkage relationships and gene order around the locus for X-linked retinoschisis. Am J Hum Genet 1988;43:476-83.
14. Alitalo T, Kruse TA, de la Chapelle A. Refined localisation of the gene causing X-linked juvenile retinoschisis. Genomics 1991;9:505-10.
15. Alitalo T, Kruse TA, Ahrens P, Albertsen HM, Eriksson AW, de la Chapelle A. Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region. Hum Genet 1991;86:599-603.
16. Dahl N, Goonewardena P, Chotai J, Anvret M, Pettersson U. DNA linkage analysis of X-linked retinoschisis. Hum Genet 1988;78:228-32.