Two novel deletions (array CGH findings) in pigment dispersion syndrome

Ophthalmic Genetics

Volumn 28, Issue 4, 2007, Pages 216-219

  Mikelsaar, Ruth ^a   Molder, Harras ^b   Bartsch, Oliver ^c   Punab, Margus ^d  

^a UNIVERSITY OF TARTU   (Estonia)

^b Joint Stock Company of Ophthalmic Surgery   (Estonia)

^c JOHANNES GUTENBERG UNIVERSITY   (Germany)

^d TARTU UNIVERSITY CLINICS   (Estonia)

Author keywords

Array CGH; Balanced translocation t(10; 15); FISH; Pigment dispersion syndrome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; DNA SEQUENCE; EYE DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE TRANSLOCATION; HUMAN; MALE; PIGMENT DISORDER; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 15; EYE DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NUCLEIC ACID HYBRIDIZATION; PIGMENT EPITHELIUM OF EYE; RETINAL PIGMENTS; SEQUENCE DELETION; TRANSLOCATION, GENETIC;

EID: 37649022743     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.1080/13816810701635269     Document Type: Article

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