Ocular findings in the chromosome 22q11.2 deletion syndrome

Journal of AAPOS

Volumn 11, Issue 2, 2007, Pages 179-182

  Forbes, Brian J ^a,b   Binenbaum, Gil ^a,b   Edmond, Jane C ^c   DeLarato, Nicole ^d   McDonald McGinn, Donna M ^a   Zackai, Elaine H ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c TEXAS CHILDREN S HOSPITAL   (United States)

^d ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AMBLYOPIA; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; CONTROLLED STUDY; EMBRYOTOXICITY; EYE DISEASE; EYE EXAMINATION; EYELID DISEASE; FEMALE; FOLLOW UP; HUMAN; INCIDENCE; INFANT; MAJOR CLINICAL STUDY; MALE; OPHTHALMOLOGY; OPTIC NERVE DISEASE; PRIORITY JOURNAL; PTOSIS; RETINA BLOOD VESSEL; STRABISMUS;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; EYE ABNORMALITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MALE; PROSPECTIVE STUDIES;

EID: 34047128675     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaapos.2006.08.006     Document Type: Article

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