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Independent variant analysis ofTEAD1andOCEL1in 38 Aicardi syndrome patients

  • Published:2017-01-25 Issue:2 Volume:5 Page:117-121
  • ISSN:2324-9269
  • Container-title:Molecular Genetics & Genomic Medicine
  • language:en
  • Short-container-title:Mol Genet Genomic Med

Author:

Wong Bibiana K. Y.12,Sutton Vernon R.3,Lewis Richard A.3456,Van den Veyver Ignatia B.123

Affiliation:

1. Department of Obstetrics and Gynecology; Baylor College of Medicine; Houston Texas

2. Jan and Dan Duncan Neurological Research Institute; Texas Children's Hospital; Houston Texas

3. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas

4. Department of Medicine; Baylor College of Medicine; Houston Texas

5. Department of Pediatrics; Baylor College of Medicine; Houston Texas

6. Department of Ophthalmology; Baylor College of Medicine; Houston Texas

Funder

Aicardi Syndrome Foundation

National Institute of Child Health and Human Development

National Center for Research Resources

GReAT (Genetic Resource Association of Texas)

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference27 articles.

1. Aicardi syndrome: old and new findings;Aicardi;Int. J. Pediatr.,1999

2. Aicardi syndrome;Aicardi;Brain Dev.,2005

3. A new syndrome: spasms in flexion, callosal agenesis, ocular abnormalities;Aicardi;Electroencephalogr. Clin. Neurophysiol.,1965

4. Helicoid peripapillary chorioretinal degeneration;Brazitikos;Am. J. Ophthalmol.,1990

5. Clinical, cytogenetic, and pedigree findings in 18 cases of Aicardi syndrome;Donnenfeld;Am. J. Med. Genet.,1989

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