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

Authors

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

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