The genetic basis of incomitant strabismus: Consolidation of the current knowledge of the genetic foundations of disease

Seminars in Ophthalmology

Volumn 28, Issue 5-6, 2013, Pages 427-437

  Graeber, Carolyn P ^a,b   Hunter, David G ^a,b   Engle, Elizabeth C ^a,b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Congenital cranial dysinnervation disorders; Congenital fibrosis of the extraocular muscles; Duane syndrome; Horizontal gaze palsy with progressive scoliosis; HOXA1; HOXB1; Incomitant strabismus; Moebius syndrome

Indexed keywords

ACRORENAL OCULAR SYNDROME; ARTICLE; ATHABASCAN BRAIN DYSGENESIS SYNDROME; AUTOSOMAL RECESSIVE INHERITANCE; BOSLEY SALIH ALORAINY SYNDROME; CHROMOSOME 12; CONGENITAL FIBROSIS OF THE EXTRAOCULAR MUSCLES; DUANE RETRACTION SYNDROME; GAZE PARALYSIS; GENE MUTATION; GENETIC DISORDER; HOLT ORAM SYNDROME; HOXA1 SYNDROME; HOXB1 SYNDROME; HUMAN; MOEBIUS SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SCOLIOSIS; STRABISMUS; SYNDROMIC DUANE SYNDROME; TOWNES BROCKS SYNDROME;

DUANE RETRACTION SYNDROME; EYE DISEASES, HEREDITARY; HOMEODOMAIN PROTEINS; HUMANS; MOBIUS SYNDROME; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; SCOLIOSIS; STRABISMUS; TRANSCRIPTION FACTORS;

EID: 84886419406     PISSN: 08820538     EISSN: 17445205     Source Type: Journal    
DOI: 10.3109/08820538.2013.825288     Document Type: Article

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