Williams syndrome: An historical perspective of its evolution, natural history, and etiology
- 6 June 2005
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 37 (S6) , 89-96
- https://doi.org/10.1002/ajmg.1320370616
Abstract
No abstract availableKeywords
This publication has 72 references indexed in Scilit:
- Natural history of Williams syndrome: Physical characteristicsThe Journal of Pediatrics, 1988
- Impaired calcitonin secretion in patients with Williams syndromeThe Journal of Pediatrics, 1985
- Systemic hypertension secondary to peripheral vascular anomalies in patients with Williams syndromeThe Journal of Pediatrics, 1985
- Observations on the evolution and treatment of idiopathic infantile hypercalcemiaThe Journal of Pediatrics, 1984
- Structure and expression of a gene encoding human calcitonin and calcitonin gene related peptideBiochemical and Biophysical Research Communications, 1984
- Characterization and regional distribution of calcitonin binding sites in the rat brainLife Sciences, 1981
- The Williams elfin facies syndromeThe Journal of Pediatrics, 1975
- The syndrome of idiopathic hypercalcemia of infancy with associated congenital heart diseaseThe Journal of Pediatrics, 1965
- Metabolic studies in a patient with idiopathic bypercalcemia of infancyThe Journal of Pediatrics, 1963
- Cardiac findings in idiopathic hypercalcemia of infancyThe Journal of Pediatrics, 1961