Case ReportCase Report
Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome
M.J. Higley, T.W. Walkiewicz, J.H. Miller, J.G. Curran and R.B. Towbin
American Journal of Neuroradiology February 2011, 32 (2) E23-E25; DOI: https://doi.org/10.3174/ajnr.A1969
M.J. Higley
T.W. Walkiewicz
J.H. Miller
J.G. Curran

References
- 1.↵
- Tischfield MA,
- Bosley TM,
- Salih MA,
- et al
- 2.↵
- Bosley TM,
- Salih MA,
- Alorainy IA,
- et al
- 3.↵
- Bosley TM,
- Alorainy IA,
- Salih MA,
- et al
- 4.↵
- Friedman BD,
- Tarby TJ,
- Holve S,
- et al
- 5.↵
- Holve S,
- Friedman B,
- Hoyme HE,
- et al
- 6.↵
- Erickson RP
- 7.↵
- Ozgen B,
- Oguz KK,
- Atas A,
- et al
- 8.↵
- Lee JH,
- Oh CW,
- Lee SH,
- et al
In this issue
Advertisement
Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome
M.J. Higley, T.W. Walkiewicz, J.H. Miller, J.G. Curran, R.B. Towbin
American Journal of Neuroradiology Feb 2011, 32 (2) E23-E25; DOI: 10.3174/ajnr.A1969
Jump to section
Related Articles
- No related articles found.
Cited By...
- No citing articles found.
This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.
More in this TOC Section
Similar Articles
Advertisement