Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomaly

Archives of Ophthalmology

Volumn 117, Issue 12, 1999, Pages 1630-1633

  Mellott, Mei L ^c   Brown Jr , Jeremiah ^c   Fingert, John H ^c   Taylor, Christine M ^c   Keech, Ronald V ^c   Sheffield, Val C ^a   Stone, Edwin M ^b  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XQ; CLINICAL FEATURE; COLOR VISION DEFECT; CONGENITAL NYSTAGMUS; FAMILY STUDY; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

EID: 0033406864     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.117.12.1630     Document Type: Article

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