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Correspondence

Patients within the broad holoprosencephaly spectrum have distinct and subtle ophthalmologic anomalies: Response to Khan†

  1. Daniel E. Pineda-Alvarez1,
  2. Benjamin D. Solomon1,
  3. Erich Roessler1,
  4. Joan Z. Balog1,
  5. Donald W. Hadley2,
  6. Wadih M. Zein3,
  7. Brian P. Brooks3,
  8. Maximilian Muenke1,*

Article first published online: 7 FEB 2012

DOI: 10.1002/ajmg.a.35207

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 158A, Issue 5, pages 1244–1245, May 2012

Additional Information

How to Cite

Pineda-Alvarez, D. E., Solomon, B. D., Roessler, E., Balog, J. Z., Hadley, D. W., Zein, W. M., Brooks, B. P. and Muenke, M. (2012), Patients within the broad holoprosencephaly spectrum have distinct and subtle ophthalmologic anomalies: Response to Khan. Am. J. Med. Genet., 158A: 1244–1245. doi: 10.1002/ajmg.a.35207

Author Information

  1. 1

    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland

  2. 2

    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland

  3. 3

    National Eye Institute, National Institutes of Health, Bethesda, Maryland

*Medical Genetics Branch, National Human Genome Research, Institute National Institutes of Health, 35 Convent Drive, Building 35 Room 1B202, Bethesda, MD 20814.

  1. †

    How to Cite this Article: Pineda-Alvarez DE, Solomon BD, Roessler E, Balog JZ, Hadley DW, Zein WM, Brooks BP, Muenke M. 2012. Patients within the broad holoprosencephaly spectrum have distinct and subtle ophthalmologic anomalies: Response to Khan. Am J Med Genet Part A. 158A:1244–1245.

Publication History

  1. Issue published online: 18 APR 2012
  2. Article first published online: 7 FEB 2012
  3. Manuscript Accepted: 30 NOV 2011
  4. Manuscript Received: 22 NOV 2011

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View Full Article (HTML) Get PDF (52K)