Ophthalmologic abnormalities in a de novo terminal 6q deletion

Ophthalmic Genetics

Volumn 31, Issue 1, 2010, Pages 1-11

  Abu Amero, Khaled K ^a   Hellani, Ali ^b   Salih, Mustafa A ^a   Hussain, Abdulkarim Al ^a   Obailan, Majed Al ^a   Zidan, Ghassan ^a   Alorainy, Ibrahim A ^c   Bosley, Thomas M ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

^b SAAD SPECIALIST HOSPITAL   (Saudi Arabia)

^c Department of Anesthesiology   (United States)

Author keywords

Chromosome deletion; Congenital nystagmus; Esotropia; Horizontal gaze anomaly; Mental retardation; Myopia; Thick cornea

Indexed keywords

TATA BINDING PROTEIN;

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 6Q; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CONGENITAL NYSTAGMUS; CONVERGENT STRABISMUS; CORNEA DISEASE; CORTICAL DYSPLASIA; EYE DISEASE; EYE MOVEMENT; EYE MOVEMENT DISORDER; GAZE; GENE DELETION; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; IMPERSISTENT ECCENTRIC GAZE; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MYOPIA; PHENOTYPE; PRIORITY JOURNAL; SAUDI ARABIA; SEIZURE;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; CONSANGUINITY; CORNEA; CORNEAL TOPOGRAPHY; EYE ABNORMALITIES; GENOTYPE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; MICROCEPHALY; MYOPIA; NYSTAGMUS, CONGENITAL; PEDIGREE; PHENOTYPE; SEIZURES;

EID: 76649086035     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.3109/13816810903312535     Document Type: Article

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