Exclusion of candidate genetic loci for Duane retraction syndrome

American Journal of Ophthalmology

Volumn 127, Issue 3, 1999, Pages 358-360

  Ott, Sandra ^a   Borchert, Mark ^a   Chung, Mina ^a   Appukuttan, Binoy ^a   Wang, Xiaoguang ^a   Weinberg, Kenneth ^a   Stout, J Timothy ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 22; CHROMOSOME 4; CHROMOSOME 8; DNA DETERMINATION; DUANE RETRACTION SYNDROME; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PEDIGREE; PRIORITY JOURNAL;

EID: 0033104606     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(98)00340-7     Document Type: Article

References (5)

1. DeRespinis P.A., Caputo A.R., Wagner R.S., Guo S. Duane's retraction syndrome. Surv Ophthalmol. 3:1993;257-288.
2. Sato S. Electromyographic study on retraction syndrome. Jpn J Ophthalmol. 4:1960;57-66.
3. Cullen P., Rodgers C.S., Callen D.F., et al. Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22. Am J Med Genet. 47:1993;925-930.
4. Chew C.K., Foster P., Hurst J.A., Salmon J.F. Duane's retraction syndrome associated with chromosome 4q27-31 segment deletion. Am J Ophthalmol. 1119:1995;807-809.
5. Vincent C., Kalatzis V., Compain S., et al. A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the bor gene. Hum Mol Genetics. 10:1994;1859-1866.