Tetrasomy 15q26: A distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?

Authors

Brynn Levy, Columbia University
David Tegay, New York College of Osteopathic Medicine
Peter Papenhausen, LabCorp, Research Triangle Park, Durham, NC
James Tepperberg, LabCorp, Research Triangle Park, Durham, NC
Odelia Nahum, Columbia University
Tammy Tsuchida, George Washington UniversityFollow
Beth A. Pletcher, University of Medicine and Dentistry of New Jersey
Leena Ala-Kokko, Connective Tissue Gene Tests, Allentown, PA
Stuart Baker, Connective Tissue Gene Tests, Allentown, PA
Barbara Frederick, Coriell Institute for Medical Research, Camden, NJ
Kurt Hirschhorn, Mount Sinai School of Medicine, New York, NY
Peter Warburton, Mount Sinai School of Medicine, New York, NY
Alan Shanske, Childrens Hospital at Montiefiore, Bronx, NY

Document Type

Journal Article

Publication Date

9-2012

Journal

Genetics in Medicine

Volume

Volume 14, Issue 9

Inclusive Pages

811-818

Keywords

Arachnodactyly--diagnosis; Chromosomes; Human; Pair 15; Craniosynostoses--diagnosis; Marfan Syndrome--diagnosis; Tetrasomy--genetics

APA Citation

Levy, B., Tegay, D., Papenhausen, P., Tepperberg, J., Nahum, O., Tsuchida, T., Pletcher, B.A., Ala-Kokko, L., Baker, S., Frederick, B., Hirschhorn, K., Warburton, P., Shanske, A. (2012). Tetrasomy 15q26: A distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?. Genetics in Medicine, 14(9), 811-818.

Peer Reviewed

1