Pediatric and Developmental Pathology

, Volume 6, Issue 3, pp 270–277

Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter Is a Variant of the Former

  • Dinesh Rakheja
  • Golder N. Wilson
  • Beverly B. Rogers

DOI: 10.1007/s10024-002-1116-4

Cite this article as:
Rakheja, D., Wilson, G. & Rogers, B. Pediatr. Dev. Pathol. (2003) 6: 270. doi:10.1007/s10024-002-1116-4

Copyright information

© 2003 Society for Pediatric Patho logy

Authors and Affiliations

  • Dinesh Rakheja
    • 1
  • Golder N. Wilson
    • 2
  • Beverly B. Rogers
    • 3
  1. 1.Department of Pathology, Mail Code 9073, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USAUS
  2. 2.Department of Pediatrics, Division of Genetics and Metabolism, Children's Medical Center and The University of Texas Southwestern Medical Center, Dallas, TX, USAUS
  3. 3.Department of Pathology, Children's Medical Center and The University of Texas Southwestern Medical Center, Dallas, TX, USAUS