Chromosome abnormalities and Williams syndrome

This publication has 4 references indexed in Scilit:

• Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance
  American Journal of Medical Genetics, 1987
• A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.
  Journal of Medical Genetics, 1986
• Impaired calcitonin secretion in patients with Williams syndrome
  The Journal of Pediatrics, 1985
• Idiopathic infantile hypercalcaemia--a continuing enigma.
  Archives of Disease in Childhood, 1984