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Arthrogryposis Multiplex Congenita and the Turner Phenotype
Ingeborg Krieger, MD;
Ceres E. Espiritu, MD
Am J Dis Child. 1972;123(2):141-144.
Abstract
We report a genetically determined syndrome of arthrogryposis multiplex congenita, pterygium formation, and facial features of the Turner phenotype in two boys and two girls, including a pair of siblings.
Author Affiliations
Detroit
From the Department of Pediatrics, Wayne State University School of Medicine, and the Children's Hospital of Michigan, Detroit.
Footnotes
Received for publication June 14, 1971; accepted Oct 7.
Reprint requests to Children's Hospital of Michigan, 3901 Beaubien St, Detroit 48201 (Dr. Krieger).
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