The Journal of Pediatrics
Volume 146, Issue 4 , Pages 537-541, April 2005

Midline defects in FG syndrome: Does tethered spinal cord contribute to the phenotype?

From Medical Genetics Institute, Steven Spielberg Pediatric Research Center, Department of Pediatrics, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California; the Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia; and Maxine Dunitz Neurosurgical Institute, Department of Pediatric Neurosurgery, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California

Received 11 June 2004; received in revised form 15 September 2004; accepted 19 October 2004.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.

 Supported by SHARE's Child Disability Center, UCLA Intercampus NIH/NIGMS Medical Genetics Training Program grant GM08243 and NIH/NICHD grant HD22657 from the US Department of Health and Human Services (J.M.G.) and NIH Clinical Research LRP MD000625-01 (J.V.).

PII: S0022-3476(04)01009-1

doi:10.1016/j.jpeds.2004.10.050

The Journal of Pediatrics
Volume 146, Issue 4 , Pages 537-541, April 2005

Article Tools

* Image Usage & Resolution